3463334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35214224-G-A

3463334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35214224-G-T

3463584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214514-G-A

3463584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214514-G-C

3463584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214514-G-T

http://identifiers.org/hco/4/GRCh38#3463591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35214521-C-A

3463591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214521-C-G

3463591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214521-C-T

http://identifiers.org/hco/4/GRCh38#3463610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35214541-C-A

3463610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214541-C-T

3463679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214645-G-A

3463679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214645-G-C

3463679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214645-G-T

http://identifiers.org/hco/4/GRCh38#3463688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35214656-C-A

3463688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214656-C-T

3463698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214671-G-A

3463698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214671-G-C

3463698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214671-G-T

3463714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214710-C-T

3463867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214815-T-C

3464015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35214965-C-T

http://identifiers.org/hco/4/GRCh38#3464060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35215007-C-A

3464060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215007-C-G

3464060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215007-C-T

3464200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215105-G-A

3464425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215295-C-T

3464481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215346-G-A

3464505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215370-G-A

3464817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215595-C-T

3464837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215611-C-T

3464886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215671-C-T

3464956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35215710-G-A

3465511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216062-G-A

3465511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216062-G-C

3465557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216127-T-C

3465579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216149-C-T

3465861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216366-C-T

3465898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216388-C-T

3465979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216456-G-A

3465995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216482-C-T

3466230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216677-C-G

3466291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35216715-G-A

http://identifiers.org/hco/4/GRCh38#3466564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35217035-C-A

3466564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35217035-C-T

3466698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35217128-T-G

http://identifiers.org/hco/4/GRCh38#3466858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35217260-A-C

3467311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35217615-T-C

3467404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35217707-C-T

3467445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35217748-G-A

http://identifiers.org/hco/4/GRCh38#3467459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35217762-C-A

3467459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35217762-C-G

3467459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35217762-C-T

http://identifiers.org/hco/4/GRCh38#3473314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35221573-C-A

3473314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221573-C-G

3473314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221573-C-T

http://identifiers.org/hco/4/GRCh38#3473349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35221615-C-A

3473349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221615-C-G

3473359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221625-G-A

http://identifiers.org/hco/4/GRCh38#3473366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35221644-C-A

3473366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221644-C-T

3473648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221920-G-A

3473648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221920-G-T

3473663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221938-G-A

3473663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221938-G-T

http://identifiers.org/hco/4/GRCh38#3473694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35221953-C-A

3473694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221953-C-G

3473694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35221953-C-T

3473765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35222024-G-A

3473765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35222024-G-T

3473772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35222031-G-T

3473786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35222042-C-T

3475068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35222780-A-T

3475172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35222886-A-G

3475172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35222886-A-T

3475207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35222917-T-C

3475241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35222939-G-C

3475265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35222964-G-A

http://identifiers.org/hco/4/GRCh38#3476421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35223873-C-A

3476421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35223873-C-T

3476552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35224005-G-T

3476567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35224021-T-C

3476567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35224021-T-G

3477626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35225793-C-T

3477661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35225841-C-T

3478889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35226875-G-A

3478976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35226948-G-A

3483309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35230411-T-G

3483326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35230428-G-C

3483326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35230428-G-T

3483560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35230611-C-T

3483666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35230735-C-G

3483666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35230735-C-T

3483816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35230886-G-A

3484030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35231076-C-T

3484425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35231385-G-A

3484425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35231385-G-T

3484459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231428-T-C

3484508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231473-G-A

3484508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231473-G-T

3484509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231474-G-A

3484509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231474-G-T

3484662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231721-G-A

3484672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231733-G-A

3484672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231733-G-T

3484675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231736-C-T

http://identifiers.org/hco/4/GRCh38#3484722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35231782-C-A

3484722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231782-C-T

http://identifiers.org/hco/4/GRCh38#3484743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35231803-C-A

3484743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35231803-C-T

3484744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35231804-A-G

3484744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35231804-A-T

3484791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231830-G-A

3484791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231830-G-T

3484807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35231864-G-T

3484818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35231871-G-A

3484818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35231871-G-C

http://identifiers.org/hco/4/GRCh38#3484929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232006-C-A

3484933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 35232010-G-A

3484933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 35232010-G-T

3484957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35232034-A-T

http://identifiers.org/hco/4/GRCh38#3485265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232292-C-A

3485265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232292-C-T

http://identifiers.org/hco/4/GRCh38#3485362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232449-A-C

3485362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232449-A-T

3485366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232453-G-A

3485366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232453-G-T

http://identifiers.org/hco/4/GRCh38#3485378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232465-C-A

3485378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35232465-C-T

http://identifiers.org/hco/4/GRCh38#3485450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232535-A-C

3485450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232535-A-G

3485450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232535-A-T

3485452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232537-T-G

3485453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232538-T-C

3485453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232538-T-G

3485486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232589-G-A

3485486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232589-G-C

3485486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232589-G-T

http://identifiers.org/hco/4/GRCh38#3485508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232611-A-C

3485508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35232611-A-G

http://identifiers.org/hco/4/GRCh38#3485606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232714-C-A

http://identifiers.org/hco/4/GRCh38#3485624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232732-C-A

3485671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232779-G-A

3485671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232779-G-T

3485713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232805-G-A

3485713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232805-G-T

http://identifiers.org/hco/4/GRCh38#3485746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35232833-C-A

3485746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232833-C-T

3485763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232852-G-A

3485763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232852-G-T

3485796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232882-T-C

3485796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232882-T-G

3485844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35232927-T-G

3485917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35233003-C-G

3489487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234250-G-A

3489498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234260-T-G

http://identifiers.org/hco/4/GRCh38#3489541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35234304-C-A

3489541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234304-C-T

http://identifiers.org/hco/4/GRCh38#3489620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35234434-C-A

3489620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234434-C-T

3489771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35234586-A-G

http://identifiers.org/hco/4/GRCh38#3489804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35234619-C-A

3489804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35234619-C-G

3489804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35234619-C-T

3489912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234770-T-C

http://identifiers.org/hco/4/GRCh38#3490053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35234912-A-C

3490056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234915-T-C

3490056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234915-T-G

http://identifiers.org/hco/4/GRCh38#3490138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35234995-C-A

3490138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234995-C-T

http://identifiers.org/hco/4/GRCh38#3490139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35234996-A-C

3490139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234996-A-G

3490139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35234996-A-T

3490173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235030-T-C

3490173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235030-T-G

http://identifiers.org/hco/4/GRCh38#3490191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35235050-C-A

3490191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235050-C-T

http://identifiers.org/hco/4/GRCh38#3490200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35235062-C-A

3490218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235080-T-C

3490247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235109-T-A

3490247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235109-T-C

3490247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235109-T-G

3490259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235121-T-C

3490271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235133-T-C

3490272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235134-T-A

3490272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235134-T-C

3490275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235137-C-T

3490301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235163-C-G

3490301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235163-C-T

3490465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235345-T-C

3490465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235345-T-G

3491772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235485-C-T

3491924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235602-G-A

3491968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235637-C-T

3492371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35235979-G-A

3492404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236018-A-G

http://identifiers.org/hco/4/GRCh38#3492455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236062-A-C

3492455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236062-A-G

3492455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236062-A-T

3492507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236104-G-A

3492507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236104-G-C

3492628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236245-G-A

3492628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236245-G-C

3492628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236245-G-T

http://identifiers.org/hco/4/GRCh38#3492655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236280-C-A

3492655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236280-C-G

3492655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236280-C-T

http://identifiers.org/hco/4/GRCh38#3492660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236281-C-A

3492660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236281-C-T

3492665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236286-G-A

3492665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236286-G-T

3492709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35236330-C-T

http://identifiers.org/hco/4/GRCh38#3492835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236451-A-C

3492835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35236451-A-G

3492893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant
orthologous variants: 35236509-G-A

3492893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant
orthologous variants: 35236509-G-C

http://identifiers.org/hco/4/GRCh38#3493024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236640-C-A

3493024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236640-C-G

3493024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236640-C-T

3493027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236643-T-C

3493054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236670-G-A

3493054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236670-G-C

3493054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236670-G-T

3493276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236895-G-A

3493276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236895-G-T

3493281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236900-G-A

3493281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236900-G-C

http://identifiers.org/hco/4/GRCh38#3493340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236959-C-A

3493340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236959-C-T

3493352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236971-A-T

3493354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236973-G-A

3493354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236973-G-C

3493375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35236991-G-A

3493375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236991-G-C

3493375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236991-G-T

http://identifiers.org/hco/4/GRCh38#3493380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35236996-C-A

3493380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35236996-C-T

3493388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35237004-G-A

3493388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35237004-G-C

3493388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35237004-G-T

3493429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 35237045-C-G

3493429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 35237045-C-T

http://identifiers.org/hco/4/GRCh38#3493520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237129-C-A

3493520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237129-C-G

3493520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237129-C-T

3493555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237158-G-A

3493573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237175-G-C

3493596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237199-G-A

3493596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237199-G-T

3493642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237242-G-A

3493642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237242-G-C

http://identifiers.org/hco/4/GRCh38#3493661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237257-C-A

3493661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237257-C-T

3493681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237269-T-A

3493681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237269-T-C

3493681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237269-T-G

http://identifiers.org/hco/4/GRCh38#3493773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237348-C-A

3493773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237348-C-T

http://identifiers.org/hco/4/GRCh38#3493778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237353-C-A

3493778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237353-C-T

http://identifiers.org/hco/4/GRCh38#3493812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237384-C-A

3493824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237396-A-T

3493892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237480-G-A

3493892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237480-G-C

3493892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237480-G-T

3493916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237492-T-A

3493916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237492-T-C

http://identifiers.org/hco/4/GRCh38#3493974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237558-C-A

3493974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237558-C-T

3493987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237576-G-A

3493987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237576-G-C

http://identifiers.org/hco/4/GRCh38#3493997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35237595-C-A

3493997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237595-C-G

3493997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237595-C-T

3494008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237613-T-A

3494008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237613-T-C

3494008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237613-T-G

3494024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237635-T-A

3494024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237635-T-C

3494024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237635-T-G

3494066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237708-G-A

3494138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237830-G-A

3494138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237830-G-C

3494139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237831-T-A

3494139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237831-T-G

3494262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237983-C-G

3494262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35237983-C-T

3494306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35238049-G-T

http://identifiers.org/hco/4/GRCh38#3494383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35238165-C-A

3494383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35238165-C-T

3494422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35238245-C-G

3494422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35238245-C-T

3494508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238334-G-A

3494508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238334-G-T

3494514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238340-T-C

3494514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238340-T-G

http://identifiers.org/hco/4/GRCh38#3494551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35238362-C-A

3494551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238362-C-T

3494553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238364-G-A

3494553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238364-G-T

3494586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238393-C-T

http://identifiers.org/hco/4/GRCh38#3494709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35238486-C-A

3494709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238486-C-T

3494893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238608-C-T

3494915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238626-G-A

3495049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238689-G-C

3495049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238689-G-T

3495091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35238724-G-A

3495414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239055-G-A

3495609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239341-T-C

3495687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239406-G-A

3495703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239431-G-A

3495703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239431-G-C

3495785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239491-C-T

3495795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239501-C-G

3495795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239501-C-T

3495956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239676-C-G

3495995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239708-G-A

3496007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239720-C-T

3496061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239789-C-T

3496284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35239995-G-A

3496570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240222-T-C

3496581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240232-G-C

http://identifiers.org/hco/4/GRCh38#3496674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35240361-A-C

3496674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240361-A-G

3496681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240362-G-C

3496681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240362-G-T

3496706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240393-G-A

3496706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240393-G-T

3496707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240394-T-A

3496707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240394-T-C

3496737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240423-G-A

3496737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240423-G-C

3496743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240429-T-G

3496768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240450-A-G

3496772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240454-T-C

3496772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240454-T-G

3496773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240455-G-A

3496800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240488-C-G

3496836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: missense variant
orthologous variants: 35240524-C-T

3496837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35240525-C-T

3496855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35240543-A-G

http://identifiers.org/hco/4/GRCh38#3496956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35240627-A-C

3496956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240627-A-G

3496956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240627-A-T

3497062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240703-G-A

3497073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240711-T-G

3497092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240730-A-G

3497092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240730-A-T

3497213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240820-T-G

3497315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240884-G-A

3497429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240963-G-A

3497490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35240999-C-G

3497547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241048-T-C

3497566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241068-C-T

3497574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241076-G-A

3497639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241123-C-T

http://identifiers.org/hco/4/GRCh38#3497694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35241172-C-A

3497694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241172-C-T

3497918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241409-C-T

http://identifiers.org/hco/4/GRCh38#3497928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35241419-C-A

3498009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241486-T-C

3498110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241600-G-A

3498152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241655-G-A

3498153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241656-G-A

3498197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241696-G-A

3498197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241696-G-C

3498362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35241880-G-C

3498507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant
orthologous variants: 35242024-G-A

http://identifiers.org/hco/4/GRCh38#3498591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35242123-A-C

3498769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35242522-G-A

3498823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35242587-G-A

3499036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35242794-C-T

http://identifiers.org/hco/4/GRCh38#3499113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35242864-A-C

3499130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35242876-G-A

http://identifiers.org/hco/4/GRCh38#3499245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35242981-C-A

3499266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, undefined
orthologous variants: 35243002-C-T

3499314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243044-G-A

http://identifiers.org/hco/4/GRCh38#3499360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#35243099-A-C

3499490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, undefined
orthologous variants: 35243214-G-C

3499501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, undefined
orthologous variants: 35243225-G-A

3499504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, undefined
orthologous variants: 35243228-G-A

3499511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, undefined
orthologous variants: 35243235-C-T

3499556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243283-C-T

3499620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243319-C-G

3499668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243368-T-C

3499862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243594-A-G

3499886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243615-G-A

3500095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243743-G-C

3500168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243815-G-A

3500168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243815-G-T

3500236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35243877-C-T

3500276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35243917-C-T

3500393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35244034-G-A

http://identifiers.org/hco/4/GRCh38#3500479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244120-C-A

3500479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244120-C-G

http://identifiers.org/hco/4/GRCh38#3500483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244124-C-A

3500483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244124-C-T

http://identifiers.org/hco/4/GRCh38#3500587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244231-C-A

3500587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244231-C-G

3500587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244231-C-T

3500597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244241-T-C

3500604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244248-G-A

3500604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244248-G-C

3500620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244268-G-A

3500620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244268-G-C

3500642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244287-G-A

3500642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244287-G-C

3500642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244287-G-T

3500680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244328-G-A

3500680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron variant
orthologous variants: 35244328-G-C

3500689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35244337-C-T

3500693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 35244341-G-C

3500726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35244374-C-T

3500735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35244383-C-G

3500735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35244383-C-T

3500768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35244416-A-T

3500786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: synonymous variant
orthologous variants: 35244434-G-A

http://identifiers.org/hco/4/GRCh38#3500850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244486-C-A

3500876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244514-T-C

3500902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244552-G-T

http://identifiers.org/hco/4/GRCh38#3500949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244622-C-A

3500949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244622-C-T

3500950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244623-A-G

3500965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244638-G-A

3500965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244638-G-C

3500965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244638-G-T

http://identifiers.org/hco/4/GRCh38#3501063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244784-C-A

3501063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244784-C-T

3501110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244831-A-G

http://identifiers.org/hco/4/GRCh38#3501115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244836-C-A

3501115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244836-C-T

3501214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244927-G-A

3501214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244927-G-T

http://identifiers.org/hco/4/GRCh38#3501234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#35244946-C-A

3501234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244946-C-T

3501263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35244960-G-T

3501351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35245001-T-C

3501351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35245001-T-G

3501402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35245049-T-A

3501402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26594
most severe consequence: 3 prime UTR variant
orthologous variants: 35245049-T-C