| 8624754 | CV79868 | single nucleotide variant | NM_002001.3(FCER1A):c.15G>A (p.Met5Ile) | Malignant melanoma [RCV000059944] | not provided | 1 | 159302379 | 159302379 | Human | | name |
| 8624755 | CV79869 | single nucleotide variant | NM_002001.3(FCER1A):c.114G>A (p.Trp38Ter) | Malignant melanoma [RCV000059945] | not provided | 1 | 159303965 | 159303965 | Human | | name |
| 598228758 | CV3958994 | single nucleotide variant | NM_001387280.1(FCER1A):c.83A>G (p.Gln28Arg) | not specified [RCV005341970] | uncertain significance | 1 | 159303934 | 159303934 | Human | | name |
| 15183688 | CV718296 | single nucleotide variant | NM_001387280.1(FCER1A):c.324C>T (p.Val108=) | not provided [RCV000886280] | benign | 1 | 159304175 | 159304175 | Human | | name |
| 156108495 | CV2304260 | single nucleotide variant | NM_001387280.1(FCER1A):c.184A>G (p.Thr62Ala) | not specified [RCV004170272] | uncertain significance | 1 | 159304035 | 159304035 | Human | | name |
| 156166662 | CV2315250 | single nucleotide variant | NM_001387280.1(FCER1A):c.206G>A (p.Ser69Asn) | not specified [RCV004167239] | uncertain significance | 1 | 159304057 | 159304057 | Human | | name |
| 329372824 | CV2434030 | single nucleotide variant | NM_001387280.1(FCER1A):c.200A>G (p.Asn67Ser) | not specified [RCV004249933] | uncertain significance | 1 | 159304051 | 159304051 | Human | | name |
| 15111423 | CV706767 | single nucleotide variant | NM_001387280.1(FCER1A):c.251A>G (p.Lys84Arg) | not provided [RCV000961103] | benign | 1 | 159304102 | 159304102 | Human | | name |
| 156182103 | CV2246394 | single nucleotide variant | NM_001387280.1(FCER1A):c.415G>A (p.Asp139Asn) | not specified [RCV004107826] | likely benign | 1 | 159306071 | 159306071 | Human | | name |
| 156177295 | CV2278341 | single nucleotide variant | NM_001387280.1(FCER1A):c.385T>A (p.Phe129Ile) | not specified [RCV004147633] | uncertain significance | 1 | 159306041 | 159306041 | Human | | name |
| 156133628 | CV2284594 | single nucleotide variant | NM_001387280.1(FCER1A):c.374G>T (p.Gly125Val) | not specified [RCV004140759] | uncertain significance | 1 | 159306030 | 159306030 | Human | | name |
| 155971367 | CV2334207 | single nucleotide variant | NM_001387280.1(FCER1A):c.725G>C (p.Gly242Ala) | not specified [RCV004186193] | uncertain significance | 1 | 159307883 | 159307883 | Human | | name |
| 156330579 | CV2339501 | single nucleotide variant | NM_001387280.1(FCER1A):c.724G>T (p.Gly242Cys) | not specified [RCV004194167] | uncertain significance | 1 | 159307882 | 159307882 | Human | | name |
| 156154600 | CV2388724 | single nucleotide variant | NM_001387280.1(FCER1A):c.734T>G (p.Leu245Arg) | not specified [RCV004239593] | uncertain significance | 1 | 159307892 | 159307892 | Human | | name |
| 329379036 | CV2443268 | single nucleotide variant | NM_001387280.1(FCER1A):c.734T>A (p.Leu245His) | not specified [RCV004260072] | uncertain significance | 1 | 159307892 | 159307892 | Human | | name |
| 401777728 | CV2704301 | single nucleotide variant | NM_001387280.1(FCER1A):c.418G>A (p.Val140Met) | not specified [RCV004311287] | uncertain significance | 1 | 159306074 | 159306074 | Human | | name |
| 401738688 | CV2721950 | single nucleotide variant | NM_001387280.1(FCER1A):c.474C>A (p.Asn158Lys) | not specified [RCV004326446] | uncertain significance | 1 | 159306130 | 159306130 | Human | | name |
| 401887534 | CV2773488 | single nucleotide variant | NM_001387280.1(FCER1A):c.566C>T (p.Pro189Leu) | not specified [RCV004354118] | uncertain significance | 1 | 159306222 | 159306222 | Human | | name |
| 405724365 | CV3260599 | single nucleotide variant | NM_001387280.1(FCER1A):c.361G>A (p.Val121Met) | not specified [RCV004389201] | uncertain significance | 1 | 159306017 | 159306017 | Human | | name |
| 405724372 | CV3260600 | single nucleotide variant | NM_001387280.1(FCER1A):c.406A>G (p.Arg136Gly) | not specified [RCV004389202] | uncertain significance | 1 | 159306062 | 159306062 | Human | | name |
| 405724380 | CV3260601 | single nucleotide variant | NM_001387280.1(FCER1A):c.503T>C (p.Val168Ala) | not specified [RCV004389203] | uncertain significance | 1 | 159306159 | 159306159 | Human | | name |
| 407482571 | CV3442702 | single nucleotide variant | NM_001387280.1(FCER1A):c.571A>C (p.Asn191His) | not specified [RCV004618402] | uncertain significance | 1 | 159306227 | 159306227 | Human | | name |
| 597724297 | CV3675834 | single nucleotide variant | NM_001387280.1(FCER1A):c.626C>T (p.Pro209Leu) | not specified [RCV004919082] | uncertain significance | 1 | 159307784 | 159307784 | Human | | name |
| 597724308 | CV3675835 | single nucleotide variant | NM_001387280.1(FCER1A):c.319G>A (p.Glu107Lys) | not specified [RCV004919083] | uncertain significance | 1 | 159304170 | 159304170 | Human | | name |
| 598228767 | CV3958995 | single nucleotide variant | NM_001387280.1(FCER1A):c.425A>G (p.Lys142Arg) | not specified [RCV005341971] | uncertain significance | 1 | 159306081 | 159306081 | Human | | name |
| 15168322 | CV696197 | single nucleotide variant | NM_001387280.1(FCER1A):c.530C>T (p.Thr177Met) | not provided [RCV000949233] | benign | 1 | 159306186 | 159306186 | Human | | name |
| 15190087 | CV696198 | single nucleotide variant | NM_001387280.1(FCER1A):c.741C>A (p.Asn247Lys) | not provided [RCV000954372] | benign | 1 | 159307899 | 159307899 | Human | 1 | name |
| 15190087 | CV696198 | single nucleotide variant | NM_001387280.1(FCER1A):c.741C>A (p.Asn247Lys) | not provided [RCV000954372] | benign | 1 | 159307899 | 159307900 | Human | 1 | name |
| 15161884 | CV706768 | single nucleotide variant | NM_001387280.1(FCER1A):c.302G>A (p.Ser101Asn) | not provided [RCV000970169] | benign | 1 | 159304153 | 159304153 | Human | | name |
| 15149342 | CV706769 | single nucleotide variant | NM_001387280.1(FCER1A):c.761C>T (p.Pro254Leu) | not provided [RCV000967736] | benign | 1 | 159307919 | 159307919 | Human | | name |
