154733592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3165424-G-A

154733638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3165467-C-T

http://identifiers.org/hco/6/GRCh38#154733643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3165472-A-C

154733643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3165472-A-G

154733643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3165472-A-T

http://identifiers.org/hco/6/GRCh38#154733874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3165637-C-A

154733874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3165637-C-T

154733943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165706-G-A

154733943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165706-G-T

http://identifiers.org/hco/6/GRCh38#154733997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3165753-C-A

154733997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165753-C-T

154734054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165811-G-A

154734054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165811-G-C

154734056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165813-A-G

154734229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3165914-C-G

154735206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166604-A-G

154735262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166658-A-G

154735262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166658-A-T

154735315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166703-G-A

154735315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166703-G-C

154735348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166745-A-T

http://identifiers.org/hco/6/GRCh38#154735357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3166754-A-C

154735417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3166824-A-G

154735535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3167002-T-G

154735621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3167081-C-T

154735628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3167088-C-T

154735658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3167117-C-T

http://identifiers.org/hco/6/GRCh38#154735675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3167134-C-A

154735675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3167134-C-T

154737097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3168757-G-T

154737425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3169096-C-T

154737492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3169155-A-G

http://identifiers.org/hco/6/GRCh38#154738721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3169754-C-A

154738721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3169754-C-T

154738812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3169835-C-G

154738934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3169933-C-T

154739371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3170144-G-C

154739733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3170701-C-T

154739782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3170725-C-G

154740135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171028-A-G

154740140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171030-T-A

154740167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171062-C-T

154740251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171151-T-C

154740293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171187-C-T

154740682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171449-C-T

154740709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171477-C-T

154741272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3171986-G-C

154741850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3172225-G-C

154741850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3172225-G-T

http://identifiers.org/hco/6/GRCh38#154741925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3172297-C-A

154741925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3172297-C-G

154741925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3172297-C-T

154742236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3172619-G-T

154742943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3173246-C-T

154743251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3173513-A-G

154753717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3178531-C-T

154754535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3179359-G-A

154756680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3180951-A-G

154757350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181080-T-C

154757367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181096-G-T

154757409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181129-G-T

154757766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181428-T-C

154757788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181446-T-A

154758063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181660-A-G

http://identifiers.org/hco/6/GRCh38#154758077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3181674-A-C

154758104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3181701-G-A

154759093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3183621-T-C

154760525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3184437-T-C

154760651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3184586-T-C

154763033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3191184-C-T

154763546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3191652-A-G

154773727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3195118-A-G

154773860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3195218-T-A

154773860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3195218-T-C

154773860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3195218-T-G

154773876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3195234-A-G

154773876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3195234-A-T

154773961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3195318-G-A

154774621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3196454-A-G

154774868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3196666-C-T

http://identifiers.org/hco/6/GRCh38#154775019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3196771-A-C

154775177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3197016-T-C

154775257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3197195-A-G

154775386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3197353-T-C

154777899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3198708-G-A

154777899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3198708-G-T

http://identifiers.org/hco/6/GRCh38#154777929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3198740-C-A

154777929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3198740-C-T

154778074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3198898-T-C

154783012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3202895-C-T

154783016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3202899-A-G

154783261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3203139-A-G

154783282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3203160-T-A

154783411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3203274-C-G

154784157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3203829-A-G

154784157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3203829-A-T

154784225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3203899-T-C

154784869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3204156-C-T

154787365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3208974-A-G

154787711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209296-C-T

154787722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209307-G-T

154787890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 3209467-T-A

154788055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209618-A-G

154788055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209618-A-T

154788080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209642-T-G

154788435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3209686-T-C

154789421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3210456-T-G

154789430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3210465-T-C

154789446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3210480-T-C

154790510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3211144-T-A

154790875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3211221-T-G

154791160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3211487-A-G

154792417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3212625-A-G

http://identifiers.org/hco/6/GRCh38#154792772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3213183-C-A

154792772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3213183-C-G

154792980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213391-T-C

154792991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213402-T-C

154793044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213450-T-C

154793044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213450-T-G

154793232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213787-G-C

154793256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213811-G-A

154793343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3213894-T-A

154794870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214287-T-C

154794885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214302-A-G

154795016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3214429-T-G

154795080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3214493-A-G

154795142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214555-G-A

154795142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214555-G-T

154795183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214591-T-C

154795264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214677-G-A

154795315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214722-C-T

154795351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3214756-G-A

154801183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3215197-G-A

154801951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3218219-A-G

http://identifiers.org/hco/6/GRCh38#154802858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3218617-C-A

154803489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3219554-C-T

154803564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3219622-T-C

http://identifiers.org/hco/6/GRCh38#154803612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3219670-A-C

154803612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3219670-A-G

154803642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3219704-T-C

http://identifiers.org/hco/6/GRCh38#154803645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3219707-C-A

154803661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3219737-T-C

154803663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3219739-T-C

154803811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3219878-G-C

154803874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3219945-A-T

154803931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220003-C-T

154804112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220185-G-A

154804248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220282-T-C

154804383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220402-C-G

154804383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220402-C-T

http://identifiers.org/hco/6/GRCh38#154804433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3220450-C-A

154804433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220450-C-T

154804626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3220618-A-G

154805276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3221240-G-T

http://identifiers.org/hco/6/GRCh38#154805375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#3221384-C-A

154805375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous_variant, undefined
orthologous variants: 3221384-C-T

http://identifiers.org/hco/6/GRCh38#154805381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#3221390-A-C

154805381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous_variant, undefined
orthologous variants: 3221390-A-G

154805513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, undefined
orthologous variants: 3221509-A-G

154805559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3221538-G-A

154805559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3221538-G-T

154806039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3221950-G-A

154806136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3222031-T-C

154806506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3222358-G-A

154806529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3222385-C-T

154806538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3222394-G-C

154806677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3222513-A-T

154806712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3231011-T-C

154807712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227045-A-T

154807790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227111-C-G

154807964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227272-G-A

154807964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227272-G-T

154807990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227299-T-C

154807990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227299-T-G

http://identifiers.org/hco/6/GRCh38#154808280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3227558-C-A

154808280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227558-C-T

154808337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227616-G-A

154808337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227616-G-T

154808623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227827-G-A

154808659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227862-T-G

http://identifiers.org/hco/6/GRCh38#154808671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3227871-C-A

154808671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3227871-C-G

154808761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3227961-C-T

http://identifiers.org/hco/6/GRCh38#154808849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3228030-C-A

154808849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228030-C-G

154808849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228030-C-T

154808926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228095-G-C

154809908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228340-T-A

154809908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228340-T-C

http://identifiers.org/hco/6/GRCh38#154809922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3228359-C-A

154809922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228359-C-G

154810329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3228895-G-T

154810831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3229592-T-C

154811159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3229953-T-A

154811171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3229965-T-C

154812524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233413-A-G

154812536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233426-G-C

154812545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233435-C-T

154812717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233578-A-G

154812733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233594-C-G

154812830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233667-G-T

154812851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3233689-A-G

154814368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3234345-G-A

154814375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3234351-A-G

154814484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3234436-G-C

154814591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3234502-A-G

154814616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3234525-G-A

154814683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3234587-A-T

154815359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235035-A-G

http://identifiers.org/hco/6/GRCh38#154815611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3235256-C-A

154815792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3235415-G-A

154815839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235459-T-C

http://identifiers.org/hco/6/GRCh38#154815880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3235484-C-A

154815905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235520-A-G

154815911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235526-T-G

http://identifiers.org/hco/6/GRCh38#154815925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3235539-C-A

http://identifiers.org/hco/6/GRCh38#154815944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3235557-C-A

http://identifiers.org/hco/6/GRCh38#154815957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3235570-A-C

154815957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235570-A-T

154816026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235604-A-G

154816067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235650-G-A

154818257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235833-C-G

154818386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235940-G-A

154818386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235940-G-C

154818386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235940-G-T

154818399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235956-G-T

http://identifiers.org/hco/6/GRCh38#154818427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3235981-C-A

154818427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235981-C-T

154818428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3235982-A-G

154818454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236008-T-C

154818481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 3236038-G-A

154818481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 3236038-G-T

154818553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3236110-C-G

154818553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3236110-C-T

154818673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236231-A-G

154818678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236236-G-A

154818678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236236-G-T

154818766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236923-T-C

154818777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236935-C-T

154818840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3236994-C-G

154819067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3237166-A-G

154820131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3237819-G-T

154820320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3238007-G-A

http://identifiers.org/hco/6/GRCh38#154820375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3238038-C-A

154820401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3238060-T-A

http://identifiers.org/hco/6/GRCh38#154820460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3238128-C-A

154820460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3238128-C-T

154820490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3238153-G-A

154820490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3238153-G-T

154820513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3238176-A-T

http://identifiers.org/hco/6/GRCh38#154822501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3240631-C-A

154822692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3240775-A-T

154822787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3240877-G-A

154822924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3240994-T-C

154823176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3241239-T-C

154823532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3241487-T-G

154823777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3241724-G-A

154823777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3241724-G-T

154824292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3242150-C-G

154824292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3242150-C-T

154824319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3242177-G-A

http://identifiers.org/hco/6/GRCh38#154824322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3242180-C-A

154824345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3242203-A-G

154824351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3242209-A-G

154824429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242287-G-C

154824429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242287-G-T

154824443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242306-A-G

http://identifiers.org/hco/6/GRCh38#154824477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3242337-C-A

154824477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242337-C-T

154824479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242339-T-G

154824514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242351-G-T

154824527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3242363-C-G

154826857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3242781-A-G

http://identifiers.org/hco/6/GRCh38#154826868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3242828-A-C

154826996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3242976-G-T

154827182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3243299-G-A

154827182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3243299-G-C

http://identifiers.org/hco/6/GRCh38#154827217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3243334-C-A

154827217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3243334-C-G

154827217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3243334-C-T

154827219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3243336-A-T

154827227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3243344-A-G

154827257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243386-T-A

154827257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243386-T-C

154827292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243414-G-A

154827292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243414-G-T

http://identifiers.org/hco/6/GRCh38#154827358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3243460-C-A

154827358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243460-C-G

154827358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243460-C-T

154827359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243461-A-G

http://identifiers.org/hco/6/GRCh38#154827376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3243478-A-C

154827376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243478-A-T

154827428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243529-T-C

154827467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243559-C-T

154827763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243745-T-C

154827764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243746-A-G

154827925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243835-G-A

154828085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3243983-A-T

154828356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244279-A-G

154828464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244376-C-T

154828487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244388-G-C

154828496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244397-A-G

154828496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244397-A-T

154828499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244405-T-C

154828548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244450-C-T

154828685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244584-T-A

154828685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244584-T-C

154828953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3244845-G-C

http://identifiers.org/hco/6/GRCh38#154829999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3245201-A-C

154830164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245290-C-G

154830164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245290-C-T

154830295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245406-C-T

154830308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245419-G-A

154830373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245480-A-T

154830446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245576-G-C

154830446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245576-G-T

154830765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3245905-A-G

154830953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3246084-G-A

154831133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3246261-C-T

154831186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3246332-A-G

154831186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3246332-A-T

154831219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: intron variant
orthologous variants: 3246364-G-C

154832112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3247205-C-T

154832233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: missense variant
orthologous variants: 3247326-T-C

154832363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: 3247456-G-A

http://identifiers.org/hco/6/GRCh38#154832391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3247484-A-C

154832711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 3247804-T-A

154832732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 3247825-G-T

154832903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 3247993-G-A

154832903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 3247993-G-C

154832903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 3247993-G-T

154832906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 3247996-C-G

154832906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 3247996-C-T

154833490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3248578-G-A

154833490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3248578-G-C

154833709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3248787-A-G

154833764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3248841-A-G

http://identifiers.org/hco/6/GRCh38#154833844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3248921-C-A

154833844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3248921-C-G

http://identifiers.org/hco/6/GRCh38#154833902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#3248980-C-A

154834128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20959
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3249200-G-T