75760808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98839873-T-G

75761202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98839213-G-C

75761259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98839157-G-A

75761290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98839133-C-T

75761310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98839115-C-G

75761452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98838937-T-C

75762476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98838427-G-A

75762476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98838427-G-T

75762477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98838426-G-A

75762477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98838426-G-T

75762709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98838268-G-A

75762709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98838268-G-T

http://identifiers.org/hco/11/GRCh38#75762946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98838110-A-C

75763449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98837383-G-A

75763449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98837383-G-T

http://identifiers.org/hco/11/GRCh38#75763496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98837350-C-A

75763496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98837350-C-G

75763872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98836989-T-A

75763907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98836960-A-T

75764113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98836765-A-G

75764335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98836526-G-T

75764367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98836494-T-A

75764748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98836185-G-A

75764748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98836185-G-T

75764953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98836059-C-G

75764953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98836059-C-T

75765015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98836002-T-C

75765441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98835493-A-G

75765512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98835420-G-C

75765876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98835159-C-T

75765877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98835158-G-A

75765914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98835120-T-A

75766103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98834950-C-T

75766560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98834519-A-G

75766925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98833928-C-T

75767479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98833516-T-A

75767479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98833516-T-C

http://identifiers.org/hco/11/GRCh38#75767521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98833494-A-C

75767521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98833494-A-G

75767548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98833477-T-A

75767600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98833424-A-G

75767665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98833360-A-G

75768352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98832332-G-T

75768362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98832322-G-A

http://identifiers.org/hco/11/GRCh38#75768420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98832282-A-C

75768425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98832277-C-T

75768428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 98832274-C-T

http://identifiers.org/hco/11/GRCh38#75768440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98832263-C-A

http://identifiers.org/hco/11/GRCh38#75768521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98832184-C-A

75768521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98832184-C-G

75768521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98832184-C-T

75768540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98832165-G-A

75768540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98832165-G-T

75768563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98832142-A-G

75768601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98832103-C-G

75768601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98832103-C-T

75768691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98832011-C-G

75768691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98832011-C-T

75768772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98831932-G-A

75768772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98831932-G-C

75768772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98831932-G-T

75768773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98831930-C-T

75768784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98831919-G-A

75768784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98831919-G-C

75768784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98831919-G-T

75768943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98831766-G-A

75768943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98831766-G-T

75768950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98831759-G-A

75768950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98831759-G-T

http://identifiers.org/hco/11/GRCh38#75768980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98831728-C-A

75768980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98831728-C-G

75768980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98831728-C-T

75769163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98831531-A-G

http://identifiers.org/hco/11/GRCh38#75769253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98831170-C-A

75769253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98831170-C-T

http://identifiers.org/hco/11/GRCh38#75769259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98831164-A-C

75769259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98831164-A-G

75769659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98830697-G-A

75770325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98830144-C-T

75770536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98829985-G-A

75770536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98829985-G-T

75770537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98829984-T-C

75771179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98829338-A-G

75771499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98828915-G-A

75771631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98828783-T-C

75771705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98828697-C-T

75771825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98828609-G-A

75772456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 98827817-T-A

http://identifiers.org/hco/11/GRCh38#75774744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98826855-C-A

75774744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826855-C-T

75774931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826697-C-T

75774953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826680-A-G

75775251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826400-C-G

75775251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826400-C-T

75775261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826390-G-A

75775357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826324-C-G

75775422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826265-G-A

75775503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826187-C-T

75775504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826186-G-A

75775705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98826014-C-T

http://identifiers.org/hco/11/GRCh38#75775765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98825965-C-A

75775827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98825893-G-A

75775827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98825893-G-T

75775934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825792-A-G

http://identifiers.org/hco/11/GRCh38#75775950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98825776-C-A

75775987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825741-C-G

75776082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98825701-G-A

75776122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98825644-G-A

75776132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98825634-T-C

75776133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98825633-T-C

http://identifiers.org/hco/11/GRCh38#75776547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98825299-C-A

75776645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825237-G-A

75776690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825190-A-G

75776765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825127-T-C

75776774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825118-G-A

75776774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825118-G-T

75776776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825116-G-A

75776845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825043-T-C

75776869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98825019-G-T

75777031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824965-G-T

75777408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824656-G-A

75777566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824508-T-A

75777566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824508-T-C

75777599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824475-A-G

75777735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824362-G-A

75778088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824096-A-G

75778188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98824014-C-T

75778380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823872-C-T

75778419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823848-C-T

75778519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823766-A-G

75778519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823766-A-T

http://identifiers.org/hco/11/GRCh38#75778528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98823757-A-C

75779143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823320-C-G

75779143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823320-C-T

75779261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98823154-C-T

75779744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98822782-G-C

75779795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98822711-G-A

75779919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98822615-T-A

75779941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98822601-A-G

75780224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98822299-G-A

75780656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98821801-C-G

75780930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98821579-C-T

75781162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98821336-G-A

75781665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98821039-T-G

75781773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98820955-C-T

75781999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98820741-C-T

75782029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98820676-A-G

http://identifiers.org/hco/11/GRCh38#75782295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98820388-C-A

75782295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98820388-C-G

75782295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98820388-C-T

75783940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98819822-C-T

75784272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98819313-T-G

75784297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98819288-T-C

75784309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98819278-G-T

http://identifiers.org/hco/11/GRCh38#75784330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98819252-C-A

http://identifiers.org/hco/11/GRCh38#75784336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98819246-C-A

75784380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98819239-G-A

75784380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98819239-G-T

http://identifiers.org/hco/11/GRCh38#75784405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98819219-C-A

75784405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98819219-C-T

75784419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98819214-G-A

75784419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98819214-G-T

75784421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98819212-A-G

75784474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98819161-G-T

75784493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98819148-T-C

75784543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98819101-A-G

75784584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98819061-G-T

75784758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818893-C-G

75784758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818893-C-T

75784776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818875-G-C

75784776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818875-G-T

http://identifiers.org/hco/11/GRCh38#75784863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98818836-C-A

75784863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818836-C-G

75784863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818836-C-T

75784873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818826-G-A

75784873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818826-G-T

75784929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818774-G-T

75785085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818660-A-G

75785087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818655-G-T

75785521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818280-A-G

75785525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818276-A-G

75785531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818270-G-A

75785531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98818270-G-C

75786394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98817518-G-T

75786633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98817296-C-T

75786764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98817153-C-T

75787032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98816900-A-G

75787218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98816727-A-G

75787218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98816727-A-T

75787548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98816399-C-T

http://identifiers.org/hco/11/GRCh38#75787552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98816395-C-A

75787873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815949-G-C

75787879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815943-T-C

75787959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815847-T-A

75788093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815767-G-C

75788251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815645-A-G

75788366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815537-T-C

75788629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815322-G-A

75788874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815236-C-T

75788910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98815199-G-A

75789533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814920-G-T

75789568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814890-G-A

http://identifiers.org/hco/11/GRCh38#75789946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98814569-A-C

75789946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814569-A-G

http://identifiers.org/hco/11/GRCh38#75790073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98814462-C-A

http://identifiers.org/hco/11/GRCh38#75790128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98814438-C-A

75790128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814438-C-T

75790147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814434-G-A

75790157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814424-A-G

75790283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: missense variant
orthologous variants: 98814299-A-G

http://identifiers.org/hco/11/GRCh38#75790311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98814271-C-A

75790311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814271-C-G

75790581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98814000-G-A

75790964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98812945-A-T

75791290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, undefined
orthologous variants: 98812685-G-A

75791691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: 98812418-T-C

http://identifiers.org/hco/11/GRCh38#75792014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98812126-C-A

75792235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811908-A-G

75792339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811744-G-T

http://identifiers.org/hco/11/GRCh38#75792417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98811581-C-A

75792417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811581-C-T

75792449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811538-A-G

75792461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811526-A-G

http://identifiers.org/hco/11/GRCh38#75792494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98811488-C-A

75792497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811485-C-G

75792497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811485-C-T

75792508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811474-T-C

75792644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811348-A-G

75792655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811339-T-C

75792676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811318-A-G

75792701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811294-G-T

75792710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811285-G-A

75792710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811285-G-T

75792738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811257-G-C

75792738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811257-G-T

http://identifiers.org/hco/11/GRCh38#75792746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98811249-C-A

75792746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811249-C-G

75792746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811249-C-T

75792797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811201-C-T

75792996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811092-G-T

75793074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98811032-A-G

75793252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98810870-C-T

75793253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98810869-T-C

75793364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810760-G-T

http://identifiers.org/hco/11/GRCh38#75793365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98810759-C-A

75793725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810477-T-C

75793790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810433-G-A

75793790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810433-G-T

75793793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810430-C-T

75793947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810291-A-G

http://identifiers.org/hco/11/GRCh38#75793956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98810282-C-A

75793956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810282-C-T

http://identifiers.org/hco/11/GRCh38#75794097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98810163-C-A

75794117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810146-G-A

75794117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810146-G-T

http://identifiers.org/hco/11/GRCh38#75794236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98810050-C-A

http://identifiers.org/hco/11/GRCh38#75794239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98810047-C-A

75794239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810047-C-G

75794239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810047-C-T

75794261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810025-G-A

75794261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98810025-G-T

75794456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809847-C-T

http://identifiers.org/hco/11/GRCh38#75794462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98809841-C-A

75794493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809809-G-T

75794601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809702-A-G

75794643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809660-T-C

75794671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809632-A-G

http://identifiers.org/hco/11/GRCh38#75794676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98809627-A-C

75795342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809153-A-G

75795387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809113-T-A

75795402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809099-T-A

75795423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809078-G-C

75795423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809078-G-T

75795458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98809041-A-G

http://identifiers.org/hco/11/GRCh38#75795542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98808992-C-A

75795542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808992-C-T

75795548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808986-T-C

http://identifiers.org/hco/11/GRCh38#75795691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98808819-C-A

75795710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808801-T-C

http://identifiers.org/hco/11/GRCh38#75795747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98808765-C-A

75795747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808765-C-T

75795795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808710-G-A

http://identifiers.org/hco/11/GRCh38#75795888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98808638-C-A

75795970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808558-T-G

http://identifiers.org/hco/11/GRCh38#75796017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98808526-C-A

75796017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98808526-C-T

75796069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808478-G-A

75796069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808478-G-C

75796069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808478-G-T

75796097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808450-G-A

75796097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808450-G-T

75796132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98808422-T-A

75796195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808362-T-G

75796222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808344-A-G

75796222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808344-A-T

75796239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 98808323-A-G

75796546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98808024-C-T

75796613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807957-G-A

75796613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807957-G-T

http://identifiers.org/hco/11/GRCh38#75796615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98807955-C-A

http://identifiers.org/hco/11/GRCh38#75796618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98807952-C-A

75796648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807919-G-T

75796770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807844-G-A

75796770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807844-G-T

75796869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807807-T-A

75796869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807807-T-C

75796869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807807-T-G

http://identifiers.org/hco/11/GRCh38#75796951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98807739-C-A

http://identifiers.org/hco/11/GRCh38#75797065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98807618-C-A

75797065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98807618-C-T

http://identifiers.org/hco/11/GRCh38#75797358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98807344-C-A

75797358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98807344-C-G

75797358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98807344-C-T

75797380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98807320-C-T

75797439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98807269-A-G

75797439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98807269-A-T

75797547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98807191-G-A

75798157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98806453-G-A

75798205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98806406-G-A

75798264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98806347-G-C

75798294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 98806317-G-A

75798448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98806164-G-C

http://identifiers.org/hco/11/GRCh38#75798484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98806128-C-A

75798484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98806128-C-G

75798674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98805893-G-A

75799251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98805400-C-T

75799261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98805390-G-A

75799296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98805343-A-G

75800315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98803942-G-A

75800515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803744-C-T

http://identifiers.org/hco/11/GRCh38#75800518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98803741-C-A

75800518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803741-C-T

http://identifiers.org/hco/11/GRCh38#75800564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98803674-C-A

75800564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803674-C-T

75800657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803585-G-A

75800657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803585-G-T

75800862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803413-A-G

http://identifiers.org/hco/11/GRCh38#75800926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98803389-C-A

75800938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803377-G-A

75800938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803377-G-C

75800938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803377-G-T

75800939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803376-G-T

75800940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803375-A-G

75800948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803367-C-T

75800969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803348-G-C

http://identifiers.org/hco/11/GRCh38#75800974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98803343-C-A

75800974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803343-C-T

75801132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 98803218-A-G

75801166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803186-G-A

75801216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 98803149-G-T

http://identifiers.org/hco/11/GRCh38#75801352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#98803035-C-A

75801352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98803035-C-G

75801352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98803035-C-T

http://identifiers.org/hco/11/GRCh38#75801378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#98803005-C-A

75801391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 16940
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98802992-T-C