114611232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 63476732-G-A

http://identifiers.org/hco/9/GRCh38#114611246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63476746-C-A

114611418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63476855-G-A

114611418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63476855-G-T

http://identifiers.org/hco/9/GRCh38#114611425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63476862-C-A

114611425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63476862-C-G

http://identifiers.org/hco/9/GRCh38#114611490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63476910-C-A

114611490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63476910-C-T

114611602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477012-G-A

114611602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477012-G-C

http://identifiers.org/hco/9/GRCh38#114611646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63477041-C-A

114611646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477041-C-T

114611677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477062-G-A

114611677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477062-G-T

114611701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477064-G-T

114611755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477092-C-G

114611825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63477132-G-A

114612241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63477524-T-C

114613007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63478117-T-G

114613015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63478125-A-G

114613300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63478403-C-T

114613460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63478525-G-A

114613472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63478537-C-T

114613583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63478626-C-T

114614473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63479135-T-C

114614590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63479243-A-G

114614592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63479245-C-G

114614592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63479245-C-T

114614606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63479261-G-A

114614606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63479261-G-C

http://identifiers.org/hco/9/GRCh38#114617266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63480833-C-A

114617332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63480913-C-T

114617333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63480914-T-C

114618883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63481547-C-T

114619100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63481750-T-A

114619100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63481750-T-C

114619211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63481841-C-T

114619242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63481872-C-T

114619354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63481927-A-G

114620752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63482564-A-G

http://identifiers.org/hco/9/GRCh38#114620917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63482692-C-A

114620917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63482692-C-T

114623988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63483592-C-G

114623988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63483592-C-T

http://identifiers.org/hco/9/GRCh38#114624025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63483630-C-A

114624037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63483642-G-A

114624037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63483642-G-T

http://identifiers.org/hco/9/GRCh38#114624099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63483688-A-C

114624099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63483688-A-G

114624099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63483688-A-T

114624217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63483776-A-G

114624220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63483779-G-T

http://identifiers.org/hco/9/GRCh38#114624276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63483828-C-A

http://identifiers.org/hco/9/GRCh38#114624296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63483837-A-C

114624296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63483837-A-G

http://identifiers.org/hco/9/GRCh38#114624317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63483862-C-A

114624317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63483862-C-G

114624317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63483862-C-T

http://identifiers.org/hco/9/GRCh38#114624405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63483949-C-A

114624405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63483949-C-T

114624566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484105-G-A

114624579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484118-A-G

114624650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484174-T-G

http://identifiers.org/hco/9/GRCh38#114624662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63484186-C-A

114624754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484275-C-T

114624784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484305-A-G

114624788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484309-A-G

114624812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484334-G-A

114624823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484345-A-G

http://identifiers.org/hco/9/GRCh38#114624864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63484375-C-A

114624864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484375-C-T

114624908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484417-G-T

114624914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484423-G-A

114624977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484484-A-G

114625030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484531-T-C

http://identifiers.org/hco/9/GRCh38#114625270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63484762-C-A

114625272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484764-A-G

114625393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63484850-T-A

114626344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486088-G-A

114626667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486434-G-A

114626706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486473-C-G

114626706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486473-C-T

114626755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486525-G-T

114626800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486570-G-A

114626800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486570-G-C

114626800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486570-G-T

http://identifiers.org/hco/9/GRCh38#114626803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63486573-C-A

114626819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486589-C-T

http://identifiers.org/hco/9/GRCh38#114626826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63486596-C-A

http://identifiers.org/hco/9/GRCh38#114626884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63486685-C-A

114626884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486685-C-T

http://identifiers.org/hco/9/GRCh38#114626891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63486692-C-A

114626891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 63486692-C-T

http://identifiers.org/hco/9/GRCh38#114627067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63486843-C-A

114627088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486864-G-T

114627107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486872-T-C

114627107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486872-T-G

http://identifiers.org/hco/9/GRCh38#114627137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63486896-C-A

114627137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486896-C-T

114627180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63486918-A-G

114627379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63487068-A-G

http://identifiers.org/hco/9/GRCh38#114627426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63487116-A-C

114627426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63487116-A-G

114627507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63487192-C-G

114627716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63487373-T-C

http://identifiers.org/hco/9/GRCh38#114627842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63487498-C-A

114628001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63488089-A-G

114628021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63488106-T-C

114628021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63488106-T-G

114628449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63488798-T-C

http://identifiers.org/hco/9/GRCh38#114628542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63488904-C-A

http://identifiers.org/hco/9/GRCh38#114628605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63488967-A-C

114628605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63488967-A-G

114628695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489040-T-C

114629079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489368-A-G

114629251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489500-G-A

http://identifiers.org/hco/9/GRCh38#114629348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63489569-A-C

114629348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489569-A-G

114629571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489641-C-G

114629571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489641-C-T

114629858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489910-A-T

114629879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63489931-A-G

114630075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63490118-G-A

114630572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63490444-C-G

114630647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63490519-C-T

114630688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63490551-G-A

114630804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63490667-A-G

http://identifiers.org/hco/9/GRCh38#114630805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63490668-C-A

114630817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63490680-C-T

114632164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63491489-G-T

114632491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63491785-A-G

http://identifiers.org/hco/9/GRCh38#114632525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63491819-A-C

114633669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63495945-T-C

114633670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63495946-G-T

114633744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496014-A-G

114633744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496014-A-T

114633748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496018-G-A

114633748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496018-G-C

114633836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63496106-G-A

114633892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496162-T-C

114633894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496164-G-A

114633897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496168-A-G

114633961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496213-G-A

114633961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496213-G-T

http://identifiers.org/hco/9/GRCh38#114634164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63496294-C-A

114634328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496413-C-T

http://identifiers.org/hco/9/GRCh38#114634343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63496423-A-C

114634505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496565-G-A

114634751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496890-A-G

114634775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496914-G-A

114634850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63496993-A-G

114634863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497006-G-A

114634957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497077-T-C

114635739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497200-A-G

114635957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497399-T-C

114636207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497591-G-C

114636211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497594-G-A

114636490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

114636840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63497928-T-G

http://identifiers.org/hco/9/GRCh38#114636895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63498056-C-A

114636895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498056-C-T

114636910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498073-A-T

114636946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498115-G-A

114636946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498115-G-T

114636981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498161-T-A

114638564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63498550-G-A

114638564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63498550-G-T

114638621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63498604-T-G

114638687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63498670-G-T

http://identifiers.org/hco/9/GRCh38#114638735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63498717-C-A

114638735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498717-C-T

http://identifiers.org/hco/9/GRCh38#114638764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63498745-C-A

114638764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498745-C-T

114638791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498755-T-C

114638800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498768-T-A

114638800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498768-T-C

http://identifiers.org/hco/9/GRCh38#114638810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63498778-C-A

114638810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63498778-C-T

114638964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63499185-G-A

114638966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63499187-T-A

114639456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63499647-G-A

114639556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63499711-C-G

114640171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63499908-C-T

114640402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63500127-T-C

114640611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63500309-A-T

114640879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63500506-C-G

114640885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63500512-T-C

http://identifiers.org/hco/9/GRCh38#114640968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63500585-C-A

114641020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63500636-C-T

114641066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63500698-G-A

114641367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63501044-A-G

114641374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63501052-G-A

114641513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63501154-C-G

114642516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63501547-G-C

http://identifiers.org/hco/9/GRCh38#114643070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63501935-C-A

114643081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63501946-T-C

114643298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63502187-G-A

114643298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63502187-G-T

http://identifiers.org/hco/9/GRCh38#114643383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63502272-C-A

114643383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63502272-C-T

114643409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502294-G-T

http://identifiers.org/hco/9/GRCh38#114643466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63502351-C-A

114643466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502351-C-T

http://identifiers.org/hco/9/GRCh38#114643517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63502385-C-A

114643517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502385-C-G

114643517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502385-C-T

http://identifiers.org/hco/9/GRCh38#114643518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63502386-C-A

114643518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502386-C-G

114643581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502424-T-C

114643581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502424-T-G

114643583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502426-A-T

114643606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502448-G-T

114643636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502466-A-G

114643646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502476-A-G

114643656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502486-A-G

http://identifiers.org/hco/9/GRCh38#114643721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63502513-C-A

114643734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502526-G-T

114643751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502543-G-A

114643767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502559-A-G

114643767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502559-A-T

114643799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502590-A-G

http://identifiers.org/hco/9/GRCh38#114643820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63502611-A-C

114643820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502611-A-G

114643970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502744-G-A

114644037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502806-C-T

114644047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63502815-G-T

114644096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63502858-T-C

114644283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503017-C-T

http://identifiers.org/hco/9/GRCh38#114644285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503019-C-A

114644377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503106-G-T

114644384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503113-T-C

114644432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503132-C-T

http://identifiers.org/hco/9/GRCh38#114644492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503173-C-A

114644492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503173-C-T

114644586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503268-C-T

http://identifiers.org/hco/9/GRCh38#114644629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503324-C-A

114644629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503324-C-T

114644635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503330-A-G

114644743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503416-G-A

114644743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503416-G-T

http://identifiers.org/hco/9/GRCh38#114644754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503427-C-A

114644754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503427-C-T

114644783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503452-G-T

114644785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503454-G-T

114644787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503456-G-A

114644787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503456-G-T

http://identifiers.org/hco/9/GRCh38#114645223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503542-C-A

114645223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503542-C-T

114645241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503557-A-G

http://identifiers.org/hco/9/GRCh38#114645255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503571-C-A

http://identifiers.org/hco/9/GRCh38#114645275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63503592-C-A

114645304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503620-G-A

114645304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503620-G-T

114645309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503625-C-T

114645319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503642-G-T

114645519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503812-G-T

114645611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63503881-A-G

114645720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63503968-G-A

114645728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63503976-T-C

114645765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63503991-A-G

114645784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504004-C-T

114645801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504021-T-C

114645917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504124-T-C

114645966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504163-A-T

114645979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504176-T-C

http://identifiers.org/hco/9/GRCh38#114646109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63504234-C-A

114646143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504268-A-G

http://identifiers.org/hco/9/GRCh38#114646152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#63504278-C-A

114646152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504278-C-T

114646188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504298-G-A

114646192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504302-G-A

114646192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504302-G-T

114646228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24513
most severe consequence: 3 prime UTR variant
orthologous variants: 63504310-A-G