37950033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79933700-C-G

37950047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79933714-T-C

http://identifiers.org/hco/2/GRCh38#37950074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79933741-C-A

37950074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79933741-C-T

37950118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79933782-G-T

http://identifiers.org/hco/2/GRCh38#37950341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79933982-C-A

37950341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 79933982-C-G

37950371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 79934012-A-G

37950374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 79934015-T-A

37950374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 79934015-T-G

37950388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934029-G-A

37950388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934029-G-T

37950545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79934185-G-A

37950545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79934185-G-T

http://identifiers.org/hco/2/GRCh38#37950621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79934285-A-C

37950621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934285-A-G

http://identifiers.org/hco/2/GRCh38#37950734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79934394-C-A

37950734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934394-C-G

37950734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934394-C-T

37950743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934404-T-A

37950743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934404-T-C

37950950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934613-G-T

37951012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934674-G-A

37951065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934726-T-C

37951092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934752-T-C

37951220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934849-T-C

http://identifiers.org/hco/2/GRCh38#37951225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79934854-A-C

37951225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79934854-A-T

37951301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79934956-A-G

37951582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935210-C-T

37951723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935351-G-A

37951723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935351-G-T

http://identifiers.org/hco/2/GRCh38#37951765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79935393-A-C

37951765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935393-A-G

http://identifiers.org/hco/2/GRCh38#37951795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79935423-A-C

37951795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935423-A-G

37951795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935423-A-T

37951873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935501-A-G

http://identifiers.org/hco/2/GRCh38#37951889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79935517-C-A

37951894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935522-C-G

37951907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935535-T-C

37951950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935578-A-G

37952010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935638-T-A

37952043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935662-A-G

37952086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935702-G-A

37952087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935703-G-A

37952087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935703-G-T

37952155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935762-T-C

37952189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935796-T-C

http://identifiers.org/hco/2/GRCh38#37952306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79935925-A-C

37952306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79935925-A-G

http://identifiers.org/hco/2/GRCh38#37952518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79936113-C-A

http://identifiers.org/hco/2/GRCh38#37952594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79936182-C-A

37952594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936182-C-G

37952634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936226-T-C

37952634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936226-T-G

37952700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936278-C-T

http://identifiers.org/hco/2/GRCh38#37952704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79936282-C-A

http://identifiers.org/hco/2/GRCh38#37952771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79936332-A-C

37952949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936687-T-G

37953209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79936912-T-C

37953338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937026-A-G

37953345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937033-C-G

37953427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937106-G-A

37953430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79937109-G-C

37973498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957217-T-C

37973515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957243-A-G

37973641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957365-G-C

37973895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957582-A-G

37973989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957680-G-A

37973989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957680-G-C

37974021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957712-A-G

37974144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957835-T-C

37974160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957851-G-A

37974294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79957987-A-T

http://identifiers.org/hco/2/GRCh38#37974309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79958002-C-A

37974309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958002-C-G

37974309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958002-C-T

http://identifiers.org/hco/2/GRCh38#37974351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79958039-C-A

37974351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958039-C-G

37974428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958147-C-T

37974662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958512-A-G

37974681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958537-G-T

http://identifiers.org/hco/2/GRCh38#37974989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79958918-A-C

37974989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958918-A-G

37975025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79958953-T-A

37975162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959083-A-G

37975202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959118-T-C

37975226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959142-A-G

37975226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959142-A-T

37975280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959196-A-G

37975335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959255-A-G

37975335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959255-A-T

37975343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959263-G-A

37975343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959263-G-C

37975355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959274-A-T

37975363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959282-T-G

http://identifiers.org/hco/2/GRCh38#37975926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79959547-A-C

http://identifiers.org/hco/2/GRCh38#37976168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79959699-A-C

37976200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959721-T-A

37976413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959887-G-T

37976454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959988-G-C

37976454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79959988-G-T

37976525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79960054-A-T

http://identifiers.org/hco/2/GRCh38#37976531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79960060-A-C

37976531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79960060-A-G

37976722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79960199-A-G

37976722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79960199-A-T

37979038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79961119-G-A

37979169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79961258-T-A

37979186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79961275-C-G

37979227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79961315-G-T

37979229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79961317-G-A

37980724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966429-A-T

37980725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966430-A-G

37980919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966586-C-T

37981073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966645-C-T

http://identifiers.org/hco/2/GRCh38#37981149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79966711-C-A

37981149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966711-C-T

37981202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966761-T-A

37981202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966761-T-C

37981305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966864-T-C

37981306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966865-A-G

37981308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79966867-T-G

37981341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79966900-G-A

37981341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79966900-G-C

37981807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79968165-A-G

37981865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79968222-G-T

37981936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79968319-A-T

http://identifiers.org/hco/2/GRCh38#37981947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79968327-C-A

37982019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79968420-A-T

37982921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79969372-C-G

37982981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79969427-A-G

37983452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79969820-C-T

37983501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79969865-C-T

37984179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79970769-G-T

37984242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79970838-C-T

37984505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971090-A-G

37984797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971452-A-G

http://identifiers.org/hco/2/GRCh38#37984810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79971465-A-C

37984810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971465-A-T

http://identifiers.org/hco/2/GRCh38#37984818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79971472-C-A

37984938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971586-G-A

37985047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971691-A-G

37985141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971789-G-T

37985143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79971791-G-A

http://identifiers.org/hco/2/GRCh38#37985194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79971834-C-A

37988351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973184-A-G

37988424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973253-A-G

37988485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973296-G-A

37988535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973341-C-T

37988568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973384-A-G

37988598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973415-G-A

37988642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973455-C-G

37988642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973455-C-T

37988733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973539-A-G

37988924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973723-G-T

37988976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79973778-G-C

37989259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974007-T-C

37989275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974022-A-G

37989394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974144-T-G

37989403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974150-G-T

http://identifiers.org/hco/2/GRCh38#37989425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79974172-A-C

37989425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974172-A-G

37989425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974172-A-T

37989469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974218-T-C

37989469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974218-T-G

37989472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974221-T-C

37989481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974230-G-A

37989481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974230-G-T

http://identifiers.org/hco/2/GRCh38#37989712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79974390-C-A

37989743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974417-G-C

37989743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974417-G-T

37989838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974502-G-A

http://identifiers.org/hco/2/GRCh38#37990642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79974892-A-C

37990664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79974914-T-G

http://identifiers.org/hco/2/GRCh38#37990842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79975106-A-C

37990918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975160-T-A

37990918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975160-T-C

37991166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975328-A-G

37991166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975328-A-T

37991208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975366-T-A

37991208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975366-T-C

http://identifiers.org/hco/2/GRCh38#37991285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79975445-A-C

37991285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975445-A-G

37991285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975445-A-T

http://identifiers.org/hco/2/GRCh38#37991288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79975448-C-A

37991288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975448-C-G

37991288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975448-C-T

37991297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79975457-T-A

37991297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79975457-T-C

37991297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 79975457-T-G

37991306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975465-A-G

37991312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975471-T-A

37991312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975471-T-C

37991322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975481-A-G

37991327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975486-T-A

37991327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975486-T-C

37991373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975538-G-A

37991373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975538-G-T

37991402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975567-G-T

37991443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975599-T-C

37991573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975715-A-G

http://identifiers.org/hco/2/GRCh38#37991607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79975738-C-A

37991607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975738-C-T

37991641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79975763-C-G

37991804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79976068-A-G

37991901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79976167-T-C

37992091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79976344-T-C

http://identifiers.org/hco/2/GRCh38#37997364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79977951-C-A

37997364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79977951-C-T

37997517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79978087-A-G

37997517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79978087-A-T

37997520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79978090-T-A

37997520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79978090-T-C

38001785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978470-T-A

38002291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978681-C-T

38002387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978746-A-G

38002444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978807-G-A

38002460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978823-G-A

38002742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978971-G-A

38002742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79978971-G-C

http://identifiers.org/hco/2/GRCh38#38002906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79979125-C-A

http://identifiers.org/hco/2/GRCh38#38002990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79979189-C-A

38002990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79979189-C-T

38003021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79979220-G-A

38003139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979318-G-C

38003170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979349-G-A

38003170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979349-G-C

38003171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979350-A-G

38003629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979431-T-C

38003647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979454-G-C

38003691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979503-G-A

38003691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979503-G-C

38003716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979528-T-C

38003767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979563-G-T

38003917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979703-A-G

38004101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79979885-G-T

38004242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79980026-G-A

38004242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79980026-G-C

38004326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79980091-G-A

http://identifiers.org/hco/2/GRCh38#38004341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79980105-C-A

http://identifiers.org/hco/2/GRCh38#38004365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79980129-C-A

38004368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79980132-A-T

38011199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79986709-A-T

38011218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79986729-A-G

38011244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79986753-A-G

38011253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79986762-A-T

38011331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79986838-C-T

38011367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79986876-T-C

38011553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987047-C-T

38011605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987084-T-C

38011611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987090-G-A

38011613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987092-G-T

38011777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987252-C-T

38012264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987513-C-G

38012264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987513-C-T

38012452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987699-G-T

38012474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987720-A-T

38012574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987823-T-G

38012637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79987880-C-T

38012725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987963-C-G

38012725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987963-C-T

http://identifiers.org/hco/2/GRCh38#38012741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79987976-C-A

38012743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987978-G-A

38012743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79987978-G-T

http://identifiers.org/hco/2/GRCh38#38012757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79987992-C-A

http://identifiers.org/hco/2/GRCh38#38012787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79988020-C-A

38012787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988020-C-G

38012829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988046-A-T

38012888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988100-G-T

38012894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988106-T-C

http://identifiers.org/hco/2/GRCh38#38013049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79988262-C-A

38013049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988262-C-T

38013108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988321-A-G

38013242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988460-A-G

38013291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79988509-T-C

38017134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79989009-G-C

38017134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79989009-G-T

38017144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79989019-G-T

38017156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79989031-T-C

http://identifiers.org/hco/2/GRCh38#38017197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79989073-A-C

http://identifiers.org/hco/2/GRCh38#38017261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79989137-C-A

38017261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989137-C-G

38017261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989137-C-T

38017335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989205-G-A

38017335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989205-G-C

38017335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989205-G-T

38017399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989263-A-G

38017526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989395-A-T

38017550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989416-T-C

38017550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989416-T-G

38017623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989476-A-G

http://identifiers.org/hco/2/GRCh38#38017701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79989541-A-C

38017701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989541-A-G

38017708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989547-G-A

38017708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989547-G-C

38017708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989547-G-T

38017730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79989570-T-C

38018684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79990233-G-A

38018684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79990233-G-T

38018952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991201-G-C

38019193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991443-G-T

38019267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991533-C-G

38019267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991533-C-T

38019392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991646-T-C

38019408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991662-A-G

38019477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991731-G-A

38019508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991762-G-A

38019571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991831-C-G

38019581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79991841-T-A

38022454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79992216-C-T

38022516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79992277-G-A

38022685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79992445-A-G

38022719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79992481-A-T

38022885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79992637-A-G

38023017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79992776-T-A

38023131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79993092-G-C

38023346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79993281-G-T

38023540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79993470-G-A

38023729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79993647-T-C

38023821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79993746-A-T

38023850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79993780-G-T

http://identifiers.org/hco/2/GRCh38#38030799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79995443-C-A

38030956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995602-A-G

38030970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995616-G-A

http://identifiers.org/hco/2/GRCh38#38030971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79995617-A-C

38030992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995629-T-A

38031028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995651-T-C

38031226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995851-G-A

38031226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995851-G-C

38031226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995851-G-T

38031504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995918-A-T

38031539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79995952-A-G

38031682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996068-A-G

38031682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996068-A-T

38031950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996306-T-A

38032265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996565-G-A

38032285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996585-C-G

38032425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996726-G-T

38032500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79996777-G-C

38034132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79997656-C-G

38034301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79997825-C-T

38034320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79997841-A-G

38034591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79998097-T-A

38034880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/2/GRCh38#38035349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80000422-A-C

http://identifiers.org/hco/2/GRCh38#38035384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80000457-C-A

38035491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80000559-A-G

38035603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80000700-C-G

38035718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80000818-G-A

38035718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80000818-G-C

http://identifiers.org/hco/2/GRCh38#38035761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80000862-C-A

http://identifiers.org/hco/2/GRCh38#38035802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80000895-C-A

38035829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80000922-C-T

38035869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80000961-A-G

38035896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80000993-A-G

38035902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001004-G-C

http://identifiers.org/hco/2/GRCh38#38036007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80001101-A-C

38036007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001101-A-G

38036024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001120-G-A

38036040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001127-A-G

http://identifiers.org/hco/2/GRCh38#38036100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80001180-C-A

38036100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001180-C-T

38036106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001186-G-T

38036191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001265-C-T

38036207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001281-A-G

38036211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001285-G-A

38036211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001285-G-T

38036213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001287-A-G

38036219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001293-G-C

38036275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001328-T-C

38036295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80001349-A-G

38036350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80001399-G-A

38036408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80001431-C-T

38036483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80001507-C-T

http://identifiers.org/hco/2/GRCh38#38036497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80001521-C-A

38036602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001643-C-T

38036603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 80001644-A-G

38036667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80001707-G-A

38036834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002079-T-C

38036884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002124-G-A

38036884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002124-G-T

38036962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002190-G-C

38036994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002218-T-G

38037027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002247-C-T

38037045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002265-A-G

38037073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002293-A-G

38037252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002457-C-G

38037268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002473-A-G

38037574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002869-C-T

38037582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80002890-C-T

38037919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80003140-G-C

38038069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80003304-C-T

38038156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80003378-C-G

38038202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80003415-T-A

38038202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80003415-T-G

38038305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80003516-G-T

http://identifiers.org/hco/2/GRCh38#38038635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80003843-C-A

38038876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80004077-T-G

http://identifiers.org/hco/2/GRCh38#38044890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80005295-C-A

38044890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005295-C-G

38044891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005296-T-C

38044934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005348-C-G

38044936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005350-C-G

38045075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005506-G-T

38045162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005588-G-A

38049384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005878-G-C

38049404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005894-A-G

38049412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005902-C-G

38049439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005929-T-G

38049464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005954-T-C

38049474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80005964-C-G

38050021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006190-C-T

38050157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006317-T-C

http://identifiers.org/hco/2/GRCh38#38050198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80006358-A-C

38050207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006369-C-T

38050256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006410-C-T

38050277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006425-G-A

38050277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006425-G-T

38050296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006441-C-T

38050298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006443-C-T

38050364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006498-A-T

38050366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006500-A-G

38050457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006579-C-G

38050457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006579-C-T

38056184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006863-C-T

38056185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80006864-G-A

http://identifiers.org/hco/2/GRCh38#38056301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80007229-C-A

38056312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80007240-A-G

38056334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80007253-G-A

38056429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80007350-A-G

38056731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80007669-T-G

http://identifiers.org/hco/2/GRCh38#38056979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80008330-C-A

38057137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80008503-G-A

38057387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80008754-G-A

38057404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80008771-T-C

38058809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009081-C-G

38058813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009085-T-C

38059485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009420-G-A

38059544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009478-T-C

38059575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009495-G-T

38059668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009591-C-T

38059687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009607-G-C

38059747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009655-C-T

38059803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009709-G-A

38060325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80009830-G-A

38060514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80010014-T-A

38060802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80010243-G-A

38060814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80010258-T-C

38061348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80010798-C-T

38061452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80010907-A-G

38061472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80010928-T-A

38061552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011015-C-T

38061553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011016-T-C

38061652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011154-C-T

http://identifiers.org/hco/2/GRCh38#38061821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80011354-A-C

38061821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011354-A-T

38061958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011504-G-C

38061981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011527-C-G

38062001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011546-T-C

38062080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80011624-C-T

38062373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012022-T-A

38062380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012028-A-G

38062466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012113-T-C

38062496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012138-C-T

38065966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80012407-G-A

38065966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80012407-G-C

38066061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012492-A-G

38066061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80012492-A-T

38066466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013148-T-C

38066719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80013373-A-T

http://identifiers.org/hco/2/GRCh38#38066812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#80013460-C-A

http://identifiers.org/hco/2/GRCh38#38067007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#80013664-C-A

38067007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 80013664-C-G

38067007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41150
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 80013664-C-T