http://identifiers.org/hco/3/GRCh38#113444823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44207621-C-A

113444823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44207621-C-T

113444824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44207620-A-T

113445073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44207426-T-G

http://identifiers.org/hco/3/GRCh38#113445202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44207311-C-A

113445291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44207212-T-A

113445291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44207212-T-G

113445323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44207184-G-A

113445323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44207184-G-C

113445457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44207064-G-A

113445457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44207064-G-T

http://identifiers.org/hco/3/GRCh38#113445463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44207059-C-A

113445803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44206745-C-T

113446096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44206506-C-T

113446453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44206196-T-C

113446557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44206098-T-C

113447250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205800-G-T

113447347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205714-A-G

113447387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205683-G-A

113447411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205660-C-T

113447416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205655-A-G

http://identifiers.org/hco/3/GRCh38#113447735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44205375-A-C

113447809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205307-T-C

113447949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205206-T-C

113447984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205177-T-A

113447994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205173-T-A

113447994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205173-T-C

113448022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205154-T-A

113448022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44205154-T-C

http://identifiers.org/hco/3/GRCh38#113448174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44204998-C-A

113448200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44204968-A-G

http://identifiers.org/hco/3/GRCh38#113448223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44204945-C-A

113448223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44204945-C-T

113448236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44204931-T-A

http://identifiers.org/hco/3/GRCh38#113449456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44203478-C-A

113449458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203476-T-C

113449658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203290-C-T

113449709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203263-A-G

113449709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203263-A-T

113449774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203212-G-A

113449774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203212-G-T

http://identifiers.org/hco/3/GRCh38#113449838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44203154-C-A

113449951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203053-T-G

113449954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44203050-T-C

http://identifiers.org/hco/3/GRCh38#113450062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44202961-C-A

http://identifiers.org/hco/3/GRCh38#113450110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44202927-C-A

113450110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202927-C-T

113450135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202808-G-A

113450135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202808-G-T

113450151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202767-A-G

113450156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202762-T-G

113450179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202722-A-G

113450179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202722-A-T

113450195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202706-A-T

113450200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202701-T-C

113450206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202695-T-C

113450206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202695-T-G

113450208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202693-T-C

113450223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202678-A-G

113450223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202678-A-T

113450238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202661-T-C

113450239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202660-G-T

http://identifiers.org/hco/3/GRCh38#113450240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44202659-C-A

113450240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202659-C-T

113450298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202606-C-T

113450335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 44202564-C-T

113450467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44202429-A-G

http://identifiers.org/hco/3/GRCh38#113450566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44202347-A-C

113451539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44201549-G-A

113451921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44201272-C-T

113451990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44201190-T-G

113452089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44201077-T-C

113453289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44200222-T-C

113453365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44200166-T-C

113453430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44199735-C-T

113453496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44199671-G-C

113453496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44199671-G-T

http://identifiers.org/hco/3/GRCh38#113453692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44199475-C-A

113453706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44199461-G-A

113453719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44199448-T-C

113453844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44199323-T-C

113453938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44199229-G-A

113457444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44197077-G-T

113458039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44196508-G-A

113460579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44196192-A-G

113460618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 44196152-T-C

113460849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195932-G-A

113460849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195932-G-T

113460863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195924-A-G

113460863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195924-A-T

113460870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195917-T-A

113460871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195916-A-G

113461282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195510-T-C

113461304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195500-T-C

113461483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195349-G-T

113461618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195220-G-A

113461638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195200-T-C

113461803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44195068-G-T

113461907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44194977-A-T

http://identifiers.org/hco/3/GRCh38#113461990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44194899-A-C

113462049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44194844-G-A

113462120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44194784-G-A

113462760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44194029-G-A

113462815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193914-T-A

113462845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193884-T-A

113462856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193873-G-A

113462867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193862-T-G

113465461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193215-C-T

http://identifiers.org/hco/3/GRCh38#113465478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44193193-C-A

113465483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193188-G-A

http://identifiers.org/hco/3/GRCh38#113465512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44193159-A-C

http://identifiers.org/hco/3/GRCh38#113465594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44193082-C-A

113465594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44193082-C-T

113465702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44192977-G-T

113465774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44192905-T-C

113465776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44192903-G-T

113465828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192847-G-A

113465837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192838-T-C

113466084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192632-C-G

113466106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192610-G-T

113466201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192504-T-C

113466207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192498-G-A

113466263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192438-G-C

113466271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192430-C-G

113466271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192430-C-T

113466334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44192368-G-A

http://identifiers.org/hco/3/GRCh38#113467134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44192165-A-C

113467850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191548-T-C

113467868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191530-T-C

113467962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191476-A-G

113467964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191474-G-A

113467964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191474-G-T

113467994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191447-C-T

http://identifiers.org/hco/3/GRCh38#113468045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44191403-C-A

http://identifiers.org/hco/3/GRCh38#113468066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44191383-C-A

113468066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191383-C-G

113468066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191383-C-T

113468082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191365-A-G

113468093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191351-T-C

113468093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191351-T-G

113468095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191349-C-G

113468095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191349-C-T

http://identifiers.org/hco/3/GRCh38#113468107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44191337-A-C

113468117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191327-T-A

113468117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191327-T-G

113468268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44191177-T-C

113468320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44191125-T-C

113468339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44191106-T-C

113468424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191021-T-C

113468425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191020-T-C

113468425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191020-T-G

113468437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44191008-C-T

http://identifiers.org/hco/3/GRCh38#113468491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44190959-C-A

113468591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190871-C-T

113468615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190849-A-G

113468674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190787-T-C

113468819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44190679-T-G

113468852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 44190646-G-A

113468958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190539-T-C

113468958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190539-T-G

113469011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190488-C-G

113469011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190488-C-T

http://identifiers.org/hco/3/GRCh38#113469110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44190369-C-A

113469110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44190369-C-G

113469113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44190366-G-A

113469296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190208-A-G

113469373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190121-T-C

113469375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44190119-T-C

113469652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44189800-A-G

113469761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44189654-C-T

http://identifiers.org/hco/3/GRCh38#113469944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44189490-A-C

113488789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44188286-T-A

http://identifiers.org/hco/3/GRCh38#113488854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44188220-C-A

113488854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44188220-C-T

113488859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44188215-T-G

http://identifiers.org/hco/3/GRCh38#113488905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44188138-A-C

113488925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44188127-T-G

113489114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187950-A-G

113489123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187941-T-A

113489123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187941-T-C

113489164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187912-A-T

113489251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187843-C-G

113489251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187843-C-T

113489416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187616-A-G

113489547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187493-T-G

113489576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187472-T-C

113493108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187097-T-A

113493108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187097-T-G

113493112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187093-G-T

113493154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187051-A-G

http://identifiers.org/hco/3/GRCh38#113493169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44187036-C-A

113493169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44187036-C-T

113493248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44186958-A-G

113493336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44186867-A-G

113493381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44186821-G-T

http://identifiers.org/hco/3/GRCh38#113493598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44186631-C-A

113493945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44186160-A-G

113493945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44186160-A-T

113494130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 44185957-G-A

113494130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44185957-G-T

113494148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44185939-C-T

113494180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44185906-T-A

113494180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44185906-T-C

113494203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44185883-A-G

113494222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44185863-G-C

113494222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44185863-G-T

113494297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44185733-G-T

113494932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44185410-A-G

113495319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44182947-T-C

113495485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44182803-A-G

113498729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44179649-T-C

113498789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44179599-G-T

113498818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44179570-T-C

113498824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44179564-A-G

113498844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44179544-A-G

113498911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44179480-G-C

http://identifiers.org/hco/3/GRCh38#113499308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44178367-C-A

113499308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44178367-C-T

113499324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44178350-G-T

http://identifiers.org/hco/3/GRCh38#113499351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44178324-C-A

113499591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44178112-A-T

113499847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44177877-T-C

113499897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44177827-G-A

113499991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44177771-T-C

113500076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44177691-T-C

113500288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44177496-A-G

113503017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44176716-G-C

113503064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44176669-A-G

113503130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44176603-T-C

113503149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44176584-T-A

113503149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44176584-T-C

http://identifiers.org/hco/3/GRCh38#113503180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44176553-C-A

113506328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44176046-T-G

http://identifiers.org/hco/3/GRCh38#113506361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44176013-C-A

113506397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175982-A-G

113506409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175970-G-T

113506468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175924-G-A

113506468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175924-G-T

113506471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175921-T-A

http://identifiers.org/hco/3/GRCh38#113506583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44175823-C-A

113506583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44175823-C-G

113506583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44175823-C-T

http://identifiers.org/hco/3/GRCh38#113506655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44175758-A-C

113506669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175750-G-A

113506669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175750-G-T

113506900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175527-G-A

113506980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175469-G-A

113507131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175348-C-G

113507320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44175221-A-G

113507773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44172271-C-T

113507858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44172192-C-G

113507858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44172192-C-T

113508016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44172048-A-G

113508106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44171990-A-T

113508113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44171983-A-T

113508616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44171277-T-C

113508678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44171216-G-A

113508757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44171140-T-C

http://identifiers.org/hco/3/GRCh38#113508787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44171110-C-A

http://identifiers.org/hco/3/GRCh38#113509555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44170601-C-A

113509555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44170601-C-G

113509676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44170486-T-C

113513637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44169312-T-A

113513673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44169272-C-T

113514085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44168878-G-A

113514172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44168723-G-A

113514214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44168579-G-A

http://identifiers.org/hco/3/GRCh38#113514296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168496-C-A

http://identifiers.org/hco/3/GRCh38#113514299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168493-C-A

113514299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44168493-C-T

http://identifiers.org/hco/3/GRCh38#113514332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168461-A-C

113514368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44168432-A-G

http://identifiers.org/hco/3/GRCh38#113514370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168430-C-A

http://identifiers.org/hco/3/GRCh38#113514414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168391-C-A

113514414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44168391-C-T

http://identifiers.org/hco/3/GRCh38#113514424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168381-C-A

113514425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44168380-G-A

http://identifiers.org/hco/3/GRCh38#113514521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168312-C-A

113514658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44168206-A-G

113514660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 44168204-G-A

http://identifiers.org/hco/3/GRCh38#113514726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44168139-C-A

113514729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44168138-G-A

113514729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44168138-G-T

113514789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 44168090-C-T

113514845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44168034-G-C

113514903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44167989-T-C

113514905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44167987-T-C

113514941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44167951-A-G

113514941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44167951-A-T

http://identifiers.org/hco/3/GRCh38#113514969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44167925-C-A

113514969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44167925-C-T

113515098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44167851-T-C

113515098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44167851-T-G

http://identifiers.org/hco/3/GRCh38#113515107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44167843-C-A

http://identifiers.org/hco/3/GRCh38#113515119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44167831-A-C

http://identifiers.org/hco/3/GRCh38#113515121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#44167829-C-A

113515154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44167796-G-A

113515154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44167796-G-C

113515154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25083
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 44167796-G-T