63189634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 66826904-A-T

63189676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 66826862-G-T

http://identifiers.org/hco/15/GRCh38#63189773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66826765-A-C

63190141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66826443-G-A

63190919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66825660-G-T

63191444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66824975-T-C

63191552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66824867-T-C

http://identifiers.org/hco/15/GRCh38#63192369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#66823779-C-A

63192384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66823764-C-G

63192661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66823492-T-C

63192676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66823479-T-A

63192787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66823391-C-T

63193841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66823125-C-T

63193889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66823082-A-G

63193951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66823025-G-A

63194018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66822962-C-T

63194126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66822855-T-G

63194507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66822558-C-T

63194529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66822536-C-T

63195049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66822002-A-G

63195429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66821638-G-A

63195518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66821535-T-C

63195627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66821426-T-G

63196083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66821034-A-G

63196906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66819877-A-G

63197881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66819212-A-G

63198023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66819065-G-C

63198333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66817574-A-T

63198466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66817448-G-A

63198490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66817420-G-A

63198665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66817263-G-A

63198740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66817187-G-A

63199146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816787-C-T

63199159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816775-T-G

63199164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816770-G-C

63199199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816729-C-T

63199350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816573-C-T

63199510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816417-A-G

63199699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66816089-T-G

63199901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66815801-A-G

http://identifiers.org/hco/15/GRCh38#63200064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66815446-C-A

63200067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66815443-G-A

63200244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66815267-A-G

63200248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66815263-C-T

63200896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66815060-C-T

63201608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66814415-A-G

63201608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66814415-A-T

63201709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66814315-T-C

63201709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66814315-T-G

63201728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66814296-G-A

http://identifiers.org/hco/15/GRCh38#63202390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66813975-A-C

63202390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66813975-A-G

63202394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66813971-C-G

63202754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66813618-A-G

63203045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66813347-G-A

63203073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66813319-C-T

63203736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66812700-G-T

63204455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66812590-C-T

http://identifiers.org/hco/15/GRCh38#63204565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66812478-C-A

63204565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66812478-C-T

63204618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66812425-C-T

63204940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66812122-T-C

63205156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66811924-A-G

63205172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66811909-C-T

63205320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66811752-T-C

63205806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66811435-C-T

63206020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66810999-A-G

63206065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66810950-A-G

63206179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66810840-T-C

63206638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66810572-G-A

63207261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66810087-T-C

63207472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66809710-A-G

63208368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66808330-A-G

63210771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66807087-C-G

63210989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66806901-C-G

63211018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66806872-C-G

63211258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66806622-G-A

63211323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66806588-A-G

63211326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66806585-G-A

63211430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66806517-C-T

63212377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805729-T-C

63212390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805714-C-T

63212577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805524-G-A

63212608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805493-G-A

63212612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805489-C-T

63212712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805379-C-T

63212738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805354-A-G

63212744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66805348-T-G

63213169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66804280-T-A

63213216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66804245-G-C

63213441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66804043-C-T

63213453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66804031-T-C

63213465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66804029-G-A

63213465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66804029-G-C

http://identifiers.org/hco/15/GRCh38#63213613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66803877-A-C

63214799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66803401-T-A

63214846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66803350-A-T

63214864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66803332-G-A

63214884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66803312-A-T

63215021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66803206-C-T

63216195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66802633-T-G

63216937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66802546-C-T

63217292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66802211-G-T

63217329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66802177-G-T

63217455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66801895-C-T

63217465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66801885-A-G

63217527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66801823-T-G

http://identifiers.org/hco/15/GRCh38#63217641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66801727-A-C

63218384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796861-C-T

63218517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796759-C-G

63218846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796460-A-G

63219038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796218-G-A

63219038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796218-G-T

63220470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796218-G-A

63220470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66796218-G-T

http://identifiers.org/hco/15/GRCh38#63220699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66795045-A-C

63220699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66795045-A-G

63221031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794731-G-C

63221056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794707-G-A

63221164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794605-G-A

63221232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794532-G-A

63221389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794388-A-G

63221589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794232-C-T

63221643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66794180-C-T

63221898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66793946-T-A

http://identifiers.org/hco/15/GRCh38#63221998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66793860-A-C

63222256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66793603-C-G

63222339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66793578-G-A

63223780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66793306-G-T

63223849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 66793237-G-A

63223849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 66793237-G-T

http://identifiers.org/hco/15/GRCh38#63223850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66793236-C-A

63223850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 66793236-C-T

http://identifiers.org/hco/15/GRCh38#63224020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66793069-C-A

63224041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66793044-G-T

63224541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66792579-A-G

http://identifiers.org/hco/15/GRCh38#63224718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66791935-C-A

63224718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66791935-C-T

63225343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66790246-G-A

63225410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66790190-C-T

63227415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66789242-C-G

63227511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66789155-T-A

63227633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66789031-C-T

http://identifiers.org/hco/15/GRCh38#63227827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66788691-C-A

63227833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66788685-C-T

63228615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66788375-G-C

63229307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66787619-T-C

63229361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66787557-C-T

63229461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66787453-A-G

63231646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66784047-T-C

63231717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66783977-A-G

63231761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66783933-A-G

63232038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66783249-G-A

63232317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66783041-C-T

63232372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66781298-T-A

63233731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66780503-A-G

63233758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66780476-G-T

63234288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66779765-C-G

63234455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66779617-A-G

63234493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66779577-T-C

63235361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66778719-T-C

63238416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66775827-T-A

http://identifiers.org/hco/15/GRCh38#63238510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66775739-C-A

63238629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66775635-G-A

63238865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66775427-G-C

63238872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66775420-A-G

63239123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66774195-G-T

63239192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66774131-G-A

http://identifiers.org/hco/15/GRCh38#63239233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66774093-C-A

http://identifiers.org/hco/15/GRCh38#63242328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66772173-A-C

63244707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66770810-G-A

63245257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66770031-C-T

63245302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66769985-C-T

63245499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66769821-G-A

http://identifiers.org/hco/15/GRCh38#63248554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66769318-C-A

63248673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66769212-C-G

63248673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66769212-C-T

63249112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768664-C-G

63249337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768448-C-T

63249513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768308-G-A

63249513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768308-G-T

63249518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768304-T-A

63249518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768304-T-C

http://identifiers.org/hco/15/GRCh38#63249542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66768281-C-A

63249542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768281-C-T

63249543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768280-T-C

http://identifiers.org/hco/15/GRCh38#63249579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66768244-C-A

63249579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768244-C-T

63249636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66768186-A-G

63249791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66767998-A-G

63249862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66767915-C-T

63249893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66767849-T-A

63249893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66767849-T-C

63250338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66767196-A-G

63250415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 66767114-C-T

63250542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66766988-A-G

http://identifiers.org/hco/15/GRCh38#63250610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66766924-A-C

http://identifiers.org/hco/15/GRCh38#63250646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66766882-C-A

http://identifiers.org/hco/15/GRCh38#63250742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66766711-A-C

63250836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66766615-T-C

63250956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66766522-A-G

63250967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66766511-A-T

63251019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66766454-C-G

63251019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66766454-C-T

63251164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765927-A-G

63251251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765838-G-A

63251251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765838-G-C

http://identifiers.org/hco/15/GRCh38#63251252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66765837-A-C

63251430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66765674-G-A

63251430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66765674-G-C

63251890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66765223-A-G

63252041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66765055-C-G

63252240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66764865-G-T

63252303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66764798-T-C

63252569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66764577-G-A

63252569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66764577-G-T

63252673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66764483-T-G

63253207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66763914-G-A

63253481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66763498-T-A

63253497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66763486-G-A

63253513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66763470-A-T

63253826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66763323-T-G

63253829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66763320-C-T

63255018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66762517-G-A

63255144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66762399-T-G

63255358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66762160-C-G

63255358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66762160-C-T

63255407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66762112-G-T

63255433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 66762088-G-C

http://identifiers.org/hco/15/GRCh38#63255670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66761864-C-A

63255670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761864-C-G

63255690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761845-G-C

63255690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761845-G-T

63255716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761831-G-A

http://identifiers.org/hco/15/GRCh38#63255719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66761828-C-A

63255719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761828-C-T

63255749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761794-C-T

63255842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66761708-A-G

63256162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66760671-A-G

63256240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66760565-T-C

63256297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760503-G-A

63256402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66760401-T-G

63256445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760358-T-A

63256445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760358-T-G

63256467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760334-T-C

63256625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760176-A-G

63256688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760164-T-A

63256688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760164-T-G

http://identifiers.org/hco/15/GRCh38#63256722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#66760154-C-A

63256722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760154-C-T

63256835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 66760053-A-G

63257113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66759826-C-T

63257145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66759794-G-A

63257190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66759724-C-T

63259422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66758860-A-G

63260206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66758464-C-T

63260319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66758350-C-G

http://identifiers.org/hco/15/GRCh38#63260418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66758274-A-C

63260458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66758240-C-G

63260721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66757932-G-A

63261966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66757229-T-G

63262673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66755947-T-C

63262747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 66755873-G-A

63262747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 66755873-G-C

63262747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 66755873-G-T

63262811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66755807-T-A

http://identifiers.org/hco/15/GRCh38#63262824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66755794-C-A

63262824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66755794-C-T

http://identifiers.org/hco/15/GRCh38#63262911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66755715-C-A

63263283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66755321-A-G

63263340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66755261-C-T

63263488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66755130-A-G

http://identifiers.org/hco/15/GRCh38#63263657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66754957-C-A

63263657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 66754957-C-T

63263941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754690-G-A

63263941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754690-G-T

63264084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754546-A-G

63264216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754421-G-T

http://identifiers.org/hco/15/GRCh38#63264231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66754406-C-A

63264231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754406-C-T

63264322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754331-A-G

63264379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754277-G-T

63264480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754173-G-A

63264522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754131-T-C

63264522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754131-T-G

63264572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66754093-A-G

63265055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66753609-G-A

63265055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66753609-G-T

63265339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66753401-T-C

63265364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66753376-C-T

63265366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66753374-G-A

63265610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66753149-C-T

63266247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66752378-A-G

63266339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66752290-G-A

63266339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66752290-G-T

63266363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66752266-T-C

http://identifiers.org/hco/15/GRCh38#63266773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66751867-C-A

63267134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66751504-T-C

63267218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66751477-G-T

63267256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66751444-G-C

63267256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66751444-G-T

63267267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: 66751433-T-A

http://identifiers.org/hco/15/GRCh38#63267510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66751202-C-A

http://identifiers.org/hco/15/GRCh38#63267531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#66751180-C-A