31652405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129993111-G-A

31652405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129993111-G-T

http://identifiers.org/hco/1/GRCh38#31652766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129992768-C-A

http://identifiers.org/hco/1/GRCh38#31652882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129992652-A-C

31652943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992597-T-C

31653004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992539-G-T

31653298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992308-G-A

31653298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992308-G-T

http://identifiers.org/hco/1/GRCh38#31653346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129992260-C-A

31653346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992260-C-T

31653422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992202-G-A

31653422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992202-G-C

31653422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129992202-G-T

31653438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 129992182-A-G

31653438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 129992182-A-T

31653692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991941-T-A

31653692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991941-T-C

31653692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991941-T-G

31653715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991916-G-A

31653744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991891-G-T

31653772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991863-C-T

31653836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991799-G-A

http://identifiers.org/hco/1/GRCh38#31653861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129991768-A-C

31653861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991768-A-T

31653905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129991724-A-G

31654101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991545-G-T

31654484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129991108-C-T

31654563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990955-G-C

31654563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990955-G-T

31654581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990938-G-A

31654936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990570-A-G

31654936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990570-A-T

http://identifiers.org/hco/1/GRCh38#31654952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129990554-C-A

31654952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990554-C-G

31655150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990465-G-A

31655150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990465-G-C

http://identifiers.org/hco/1/GRCh38#31655166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129990449-C-A

31655166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990449-C-T

31655208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990420-G-A

31655214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990414-T-A

31655214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990414-T-C

31655214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990414-T-G

31655221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990407-G-A

31655281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129990360-A-T

31655438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129990201-C-T

31655451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129990188-C-G

31655508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129990131-A-G

31655515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129990110-A-G

31655625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129990009-T-C

http://identifiers.org/hco/1/GRCh38#31655661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989979-C-A

31655661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989979-C-T

http://identifiers.org/hco/1/GRCh38#31655720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989921-A-C

31655720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989921-A-G

31655859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989817-T-C

31655882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989787-T-A

http://identifiers.org/hco/1/GRCh38#31655895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989772-A-C

31655895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989772-A-G

31655904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129989763-T-C

31655904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129989763-T-G

31655909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 129989758-A-G

http://identifiers.org/hco/1/GRCh38#31655965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989695-C-A

31655965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989695-C-T

31656004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989680-G-A

31656004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989680-G-C

31656004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989680-G-T

http://identifiers.org/hco/1/GRCh38#31656005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989679-C-A

31656005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989679-C-T

31656022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989664-T-A

31656022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989664-T-C

31656043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129989643-G-A

31656043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129989643-G-C

31656076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989612-T-C

31656076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989612-T-G

http://identifiers.org/hco/1/GRCh38#31656116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989566-C-A

31656116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989566-C-T

31656174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989557-A-G

31656186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 129989545-G-A

31656186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 129989545-G-T

http://identifiers.org/hco/1/GRCh38#31656209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989529-C-A

31656209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989529-C-T

31656244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989507-G-A

31656265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989486-G-A

31656265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989486-G-T

http://identifiers.org/hco/1/GRCh38#31656278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989481-C-A

31656293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989471-C-T

31656300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989464-G-A

31656300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989464-G-T

31656431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129989347-T-C

http://identifiers.org/hco/1/GRCh38#31656454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129989317-A-C

31656520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989252-G-A

31656520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989252-G-C

31656568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989205-T-C

31656568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989205-T-G

31656612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989148-A-G

31656717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989048-C-T

31656761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129989005-G-C

31656792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129988992-T-G

31656820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129988964-G-A

31656820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129988964-G-T

31656944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988423-T-C

31656948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988419-T-C

http://identifiers.org/hco/1/GRCh38#31656998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129988371-C-A

31656998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988371-C-G

31657005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988364-G-A

http://identifiers.org/hco/1/GRCh38#31657268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129988199-C-A

http://identifiers.org/hco/1/GRCh38#31657285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129988183-C-A

31657285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988183-C-T

31657292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988176-A-G

31657292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988176-A-T

31657308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988170-A-G

http://identifiers.org/hco/1/GRCh38#31657364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129988132-C-A

31657364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129988132-C-T

31657491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129987964-A-G

31657527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987929-T-A

http://identifiers.org/hco/1/GRCh38#31657529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129987927-C-A

31657530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987926-T-A

31657530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987926-T-C

31657560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987896-G-C

31657560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987896-G-T

31657561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987884-G-A

31657561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987884-G-T

http://identifiers.org/hco/1/GRCh38#31657567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129987865-A-C

31657581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987851-G-T

31657583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987849-G-A

31657583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987849-G-C

31657583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987849-G-T

31657595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987837-G-A

31657595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987837-G-T

31657623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987793-G-A

31657623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987793-G-T

http://identifiers.org/hco/1/GRCh38#31657631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129987785-C-A

31657631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987785-C-T

31657670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987750-C-T

31657746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987680-C-T

31657800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987626-C-T

http://identifiers.org/hco/1/GRCh38#31657801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129987625-C-A

31657820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987606-G-A

31657860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987565-A-G

31657905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987517-A-G

31657928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129987494-A-G

31658240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987170-G-T

31658338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987069-G-T

http://identifiers.org/hco/1/GRCh38#31658341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129987066-C-A

31658341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129987066-C-T

http://identifiers.org/hco/1/GRCh38#31658495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129986947-C-A

31658495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129986947-C-T

31658510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129986932-G-A

31658586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986856-T-C

31658589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986853-G-A

http://identifiers.org/hco/1/GRCh38#31658591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129986851-A-C

31658599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986843-A-G

http://identifiers.org/hco/1/GRCh38#31658655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129986802-C-A

31658655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986802-C-T

31658679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986771-G-T

31658691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986760-C-T

31658826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986649-C-G

31658826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986649-C-T

31658894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986592-G-A

31658894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986592-G-C

31658915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129986571-A-G

31658915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129986571-A-T

31658923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129986563-G-A

31658923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129986563-G-C

31658923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129986563-G-T

31658997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986472-G-T

31659308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986196-C-T

31659388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986124-A-G

31659439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986045-C-T

31659445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129986039-C-G

31659489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985964-C-G

31659539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985897-G-C

http://identifiers.org/hco/1/GRCh38#31659567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129985870-A-C

31659567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985870-A-G

31659580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985858-G-A

31659581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985857-A-G

31659604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985834-C-T

31659641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985818-T-C

31659720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985766-G-A

31659720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985766-G-T

31659806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985683-A-G

31659806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985683-A-T

31659810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985679-A-G

31660026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985528-C-T

31660068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985497-G-A

31660068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985497-G-C

31660100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985466-G-A

31660163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129985433-A-G

http://identifiers.org/hco/1/GRCh38#31660291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129985326-C-A

31660329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129985289-A-T

31660462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984451-G-A

31660462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984451-G-T

31660523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984410-A-G

31660605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129984331-G-C

31660718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984221-G-C

31660736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984203-T-C

http://identifiers.org/hco/1/GRCh38#31660771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129984174-C-A

31660771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984174-C-T

31660919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129984077-A-G

http://identifiers.org/hco/1/GRCh38#31661011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129983974-C-A

31661211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983796-G-A

31661350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983628-T-C

31661494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983487-T-C

31661526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983461-C-G

31661526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983461-C-T

31661580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983407-T-A

31661580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983407-T-C

31661688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129983319-G-A

31661797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983211-A-G

31661797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983211-A-T

http://identifiers.org/hco/1/GRCh38#31661871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129983122-A-C

31661871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983122-A-G

31661902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129983091-T-C

31662017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982954-C-T

31662060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982911-C-T

31662356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129982694-T-G

31662404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982648-G-A

31662509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982551-A-G

http://identifiers.org/hco/1/GRCh38#31662541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129982526-C-A

31662541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982526-C-T

31662546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982524-G-A

31662546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129982524-G-T

http://identifiers.org/hco/1/GRCh38#31662603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129982468-C-A

31662603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129982468-C-T

31662797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982325-T-G

31662801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982321-T-C

31662801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982321-T-G

http://identifiers.org/hco/1/GRCh38#31662880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129982246-C-A

31662880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982246-C-G

31662880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982246-C-T

31663145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982109-A-G

31663225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982040-T-C

31663225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982040-T-G

http://identifiers.org/hco/1/GRCh38#31663233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129982032-C-A

31663233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982032-C-T

http://identifiers.org/hco/1/GRCh38#31663242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129982023-A-C

31663242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982023-A-G

31663254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982013-G-A

31663254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982013-G-T

31663260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982007-A-G

31663260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982007-A-T

31663264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129982002-G-A

31663310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129981955-A-G

31663356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129981905-G-T

31663413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129981864-T-C

31663413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129981864-T-G

31663489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981795-G-A

31663489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981795-G-T

31663505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981777-G-A

31663505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981777-G-T

31663574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981706-T-C

31663647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981619-C-T

31663804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981481-G-T

31664062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981288-T-C

31664329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129981080-G-A

http://identifiers.org/hco/1/GRCh38#31665020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129980466-C-A

31665060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980420-G-A

31665060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980420-G-C

31665113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980388-G-A

31665113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980388-G-T

http://identifiers.org/hco/1/GRCh38#31665125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129980378-C-A

31665158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980357-A-G

31665227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129980288-G-A

http://identifiers.org/hco/1/GRCh38#31665242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129980273-A-C

31665271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980256-G-A

31665385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980196-T-A

31665385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980196-T-C

http://identifiers.org/hco/1/GRCh38#31665446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129980165-C-A

31665446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980165-C-T

31665473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129980139-C-T

31665562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129980063-C-G

31665562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 129980063-C-T

31665689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979955-A-G

31665689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979955-A-T

31666172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129979535-G-A

31666172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129979535-G-T

31666173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129979534-G-A

31666173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129979534-G-T

31666209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129979523-C-G

31666209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129979523-C-T

31666402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979345-G-A

31666402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979345-G-T

http://identifiers.org/hco/1/GRCh38#31666405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129979342-C-A

31666455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979292-G-A

31666455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979292-G-C

31666455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979292-G-T

31666496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979254-T-C

31666496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979254-T-G

http://identifiers.org/hco/1/GRCh38#31666497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129979253-C-A

31666497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979253-C-T

http://identifiers.org/hco/1/GRCh38#31666529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129979213-C-A

31666529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979213-C-T

31666552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129979190-C-T

31666613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129979134-C-T

http://identifiers.org/hco/1/GRCh38#31666633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129979114-C-A

http://identifiers.org/hco/1/GRCh38#31666744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129978959-C-A

31666761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129978942-C-T

http://identifiers.org/hco/1/GRCh38#31666782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129978921-C-A

31666782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129978921-C-T

31666790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129978913-C-T

31666814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129978884-C-T

31666820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129978876-C-T

31667326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129978396-G-A

31667526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129978173-G-T

http://identifiers.org/hco/1/GRCh38#31667557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129978127-C-A

http://identifiers.org/hco/1/GRCh38#31667587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129978100-C-A

31667587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129978100-C-T

31667808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977861-C-T

31667897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977772-C-G

http://identifiers.org/hco/1/GRCh38#31667937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129977732-C-A

31668026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977634-G-A

31668026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977634-G-T

31668027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977633-A-T

http://identifiers.org/hco/1/GRCh38#31668085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129977580-C-A

31668085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977580-C-G

31668085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977580-C-T

31668144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977537-A-T

31668150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977531-G-T

http://identifiers.org/hco/1/GRCh38#31668301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129977401-A-C

31668472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977256-G-C

31668636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129977100-G-T

31668775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976991-T-G

31668776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976990-T-C

31668954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976818-G-A

31668954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976818-G-T

31669123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976670-C-T

31669133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976658-G-T

31669170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976621-T-C

31669263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976539-T-C

http://identifiers.org/hco/1/GRCh38#31669640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129976208-C-A

31669640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129976208-C-T

31669703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976146-T-C

http://identifiers.org/hco/1/GRCh38#31669722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129976127-C-A

31669722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129976127-C-T

http://identifiers.org/hco/1/GRCh38#31669817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129976024-C-A

31669817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129976024-C-T

http://identifiers.org/hco/1/GRCh38#31670115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129975728-C-A

http://identifiers.org/hco/1/GRCh38#31670135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129975708-C-A

31670151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129975692-G-T

http://identifiers.org/hco/1/GRCh38#31670195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129975648-C-A

31670195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975648-C-T

http://identifiers.org/hco/1/GRCh38#31670251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129975598-C-A

31670251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975598-C-T

31670408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975478-G-A

31670408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975478-G-T

http://identifiers.org/hco/1/GRCh38#31670435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129975455-C-A

31670435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975455-C-G

31670435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975455-C-T

31670502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975374-G-A

31670502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975374-G-T

31670530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975339-G-A

31670530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975339-G-T

31670699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129975173-A-G

31670721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129975158-G-A

31670721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129975158-G-T

http://identifiers.org/hco/1/GRCh38#31670722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129975157-C-A

31670728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129975151-G-A

31670728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129975151-G-T

31670892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129975024-A-G

31670948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129974974-C-T

31671139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974805-G-T

31671440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974556-C-T

31671444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974553-G-C

31671547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974476-G-T

31671685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974341-A-G

31671704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974313-A-G

31671709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974308-G-C

31671709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974308-G-T

31671769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974252-G-T

31671773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974248-C-T

31672013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129974009-A-G

31672369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129973575-A-G

31672369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129973575-A-T

31672479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129973445-A-G

31672913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972889-G-A

31672913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972889-G-C

31672913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972889-G-T

http://identifiers.org/hco/1/GRCh38#31672927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129972875-C-A

31672944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972858-G-A

31672944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972858-G-T

http://identifiers.org/hco/1/GRCh38#31672946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129972856-C-A

31672946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972856-C-G

31672946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972856-C-T

http://identifiers.org/hco/1/GRCh38#31672954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129972852-C-A

31672954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129972852-C-T

31673060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972746-G-A

31673060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972746-G-C

31673060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972746-G-T

31673097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972710-G-A

31673107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972700-T-A

31673107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972700-T-C

http://identifiers.org/hco/1/GRCh38#31673140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129972666-C-A

31673140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 129972666-C-G

31673301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129972501-T-A

31673301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129972501-T-C

31673499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129972359-G-A

31673647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129972229-G-C

31673658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129972218-G-A

31673830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129972067-T-C

31673905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971994-G-C

31673993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971903-T-C

31673997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971899-C-T

31674063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971817-T-C

31674277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971646-G-A

31674333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971612-G-A

http://identifiers.org/hco/1/GRCh38#31674639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129971392-C-A

31674639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971392-C-T

http://identifiers.org/hco/1/GRCh38#31674835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129971210-C-A

31674885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971158-T-C

31674896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971147-T-A

http://identifiers.org/hco/1/GRCh38#31674917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129971112-C-A

31674917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971112-C-T

31674918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971111-G-A

31674918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971111-G-C

31674947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129971082-G-A

31675059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970989-G-A

31675070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970978-G-A

31675072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970976-T-G

31675215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970885-G-A

31675215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970885-G-T

31675220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970881-G-A

31675418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970698-G-T

http://identifiers.org/hco/1/GRCh38#31675553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129970583-C-A

31675610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970526-G-A

31675626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970510-C-G

31676690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970091-G-A

31676706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129970075-C-G

31676869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969909-G-A

31676913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969865-T-C

31677246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969584-C-T

31677429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969521-C-T

31677707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969254-A-G

31677813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969179-G-A

31677813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129969179-G-T

31678036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129968958-C-T

31678200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129968916-T-G

31678645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129968727-G-A

31678693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129968696-A-G

31678774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129968602-A-G

31678902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129968502-G-C

http://identifiers.org/hco/1/GRCh38#31679014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129968380-A-C

http://identifiers.org/hco/1/GRCh38#31679123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129967563-C-A

31679258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129967485-A-G

31679273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129967470-G-T

31679416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129967304-T-C

31679450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129967270-C-T

31679454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 129967266-C-T

31679455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, stop_retained_variant
orthologous variants: 129967265-C-T

http://identifiers.org/hco/1/GRCh38#31679481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129967239-C-A

31679481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967239-C-T

31679492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967228-G-A

31679492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967228-G-T

31679501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967226-C-T

31679502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967225-A-G

31679540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967190-G-A

31679540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967190-G-T

http://identifiers.org/hco/1/GRCh38#31679546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129967184-C-A

31679546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967184-C-T

31679588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967135-T-C

31679588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967135-T-G

31679594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967130-C-G

31679594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129967130-C-T

31679752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129966960-A-G

http://identifiers.org/hco/1/GRCh38#31679811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129966900-C-A

31679811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: 129966900-C-T

http://identifiers.org/hco/1/GRCh38#31679835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129966876-C-A

31679835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, stop_gained
orthologous variants: 129966876-C-T

31679862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129966849-G-A

31679862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron variant
orthologous variants: 129966849-G-T

31680117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129966601-C-G

31680117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129966601-C-T

http://identifiers.org/hco/1/GRCh38#31680199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129966524-C-A

31680199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129966524-C-G

31680199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129966524-C-T

http://identifiers.org/hco/1/GRCh38#31680246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129966509-C-A

31680745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129966158-C-G

31680913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129966064-C-T

31681014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129965962-T-G

31681032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129965944-T-C

31681060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129965916-T-A

31681060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129965916-T-C

31681069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 129965904-T-C

http://identifiers.org/hco/1/GRCh38#31682860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129962618-C-A

31682913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962567-T-A

31682913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962567-T-C

31682932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 129962546-A-G

http://identifiers.org/hco/1/GRCh38#31683035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129962446-C-A

31683035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962446-C-T

31683182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962339-G-A

http://identifiers.org/hco/1/GRCh38#31683237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129962284-C-A

31683237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129962284-C-G

31683237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129962284-C-T

31683261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962260-C-G

31683325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962197-C-G

31683325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962197-C-T

31683414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962109-A-T

31683461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962069-G-A

31683461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129962069-G-C

http://identifiers.org/hco/1/GRCh38#31683565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129961451-C-A

31683565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961451-C-T

31683581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961435-G-A

31683581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961435-G-T

31683688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961337-G-A

31683689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961336-G-A

31683689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961336-G-T

31683706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 129961319-C-G

http://identifiers.org/hco/1/GRCh38#31683723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129961302-C-A

31683764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961261-G-C

31683813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961217-G-A

31683813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961217-G-C

31683892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961133-C-T

31683895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961130-A-G

31683895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961130-A-T

http://identifiers.org/hco/1/GRCh38#31683899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129961126-C-A

31683903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961122-C-G

31683914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961107-G-A

31683914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129961107-G-C

31684017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960996-G-A

31684017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960996-G-C

31684045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960968-A-G

31684120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129960895-G-C

31684293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960729-C-T

http://identifiers.org/hco/1/GRCh38#31684310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129960698-C-A

31684326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960682-T-C

31684327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960681-G-A

31684327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960681-G-T

http://identifiers.org/hco/1/GRCh38#31684330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129960678-C-A

31684330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960678-C-T

http://identifiers.org/hco/1/GRCh38#31684384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129960626-A-C

31684384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960626-A-G

http://identifiers.org/hco/1/GRCh38#31684430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129960586-C-A

31684430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960586-C-T

31684481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960541-A-T

31684482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960540-T-C

31684482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960540-T-G

http://identifiers.org/hco/1/GRCh38#31684500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129960522-C-A

31684500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960522-C-T

http://identifiers.org/hco/1/GRCh38#31684598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129960429-C-A

31684598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129960429-C-G

31684598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129960429-C-T

31684617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129960410-T-C

31684617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129960410-T-G

31684671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960356-C-T

31684679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960348-A-G

31684737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960298-G-A

31684747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960288-G-A

31684812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129960016-C-T

http://identifiers.org/hco/1/GRCh38#31684840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129959988-C-A

31684840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959988-C-G

31684840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959988-C-T

http://identifiers.org/hco/1/GRCh38#31684891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129959937-A-C

http://identifiers.org/hco/1/GRCh38#31684905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129959923-A-C

31684905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959923-A-G

31684990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959852-T-G

31685113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959745-G-T

31685353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959543-T-C

31685649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959286-G-A

http://identifiers.org/hco/1/GRCh38#31685715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129959220-C-A

31685715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959220-C-T

31685716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959219-G-A

31685716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959219-G-T

31685736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129959199-T-C

http://identifiers.org/hco/1/GRCh38#31685844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129959105-C-A

31685851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959098-A-T

31685905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959045-G-C

31685922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129959031-A-G

31686154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129958812-C-T

http://identifiers.org/hco/1/GRCh38#31686190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129958776-C-A

http://identifiers.org/hco/1/GRCh38#31686198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129958736-C-A

31686198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129958736-C-T

31686349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129958604-A-G

31686430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129958523-A-G

31686452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129958503-G-T

31686471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129958484-T-C

http://identifiers.org/hco/1/GRCh38#31686505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129958455-C-A

31688340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129956007-T-C

31688383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955972-A-T

31688410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955935-T-C

31688494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129955856-A-G

http://identifiers.org/hco/1/GRCh38#31688751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129955668-C-A

31688751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955668-C-T

31688934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129955540-G-A

31689035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955443-G-A

31689035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955443-G-T

31689041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955437-T-C

31689117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955356-A-G

31689278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955201-A-G

31689311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955183-T-A

http://identifiers.org/hco/1/GRCh38#31689314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129955180-C-A

http://identifiers.org/hco/1/GRCh38#31689325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129955170-C-A

31689325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129955170-C-T

http://identifiers.org/hco/1/GRCh38#31689423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129955052-C-A

31689423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955052-C-G

31689423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129955052-C-T

31689639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129954851-G-A

31689701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954808-T-G

31689824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 129954692-G-A

31689907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954609-G-A

31689907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954609-G-T

31689935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 129954584-T-A

31690011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954526-A-G

http://identifiers.org/hco/1/GRCh38#31690022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129954515-C-A

http://identifiers.org/hco/1/GRCh38#31690028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129954509-C-A

31690028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954509-C-G

31690028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954509-C-T

31690045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954492-G-A

31690219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954337-C-T

31690221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954335-G-A

31690221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129954335-G-T

31690413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129954192-G-T

31690422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129954183-T-A

31690442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129954147-G-A

31690634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953959-C-T

http://identifiers.org/hco/1/GRCh38#31690635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129953958-C-A

31690635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953958-C-T

31691023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953682-G-A

31691036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953667-G-T

31691053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953650-G-T

31691095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953613-T-C

http://identifiers.org/hco/1/GRCh38#31691344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129953412-C-A

31691344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953412-C-G

31691344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953412-C-T

31691345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953411-G-A

31691345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953411-G-C

31691345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953411-G-T

http://identifiers.org/hco/1/GRCh38#31691358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129953396-C-A

31691366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953388-G-A

31691366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953388-G-T

31691463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129953282-G-A

http://identifiers.org/hco/1/GRCh38#31691561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129953182-C-A

31691561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953182-C-G

http://identifiers.org/hco/1/GRCh38#31691564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129953179-C-A

31691564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953179-C-T

31691586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953157-T-C

http://identifiers.org/hco/1/GRCh38#31691744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129953000-C-A

31691744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129953000-C-T

31691837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952950-G-T

31691878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952914-T-A

31691878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952914-T-C

31691920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952876-G-A

31691920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952876-G-T

31692120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952703-T-G

31692122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952701-G-A

31692122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952701-G-T

31692148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952675-C-T

31692183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952632-G-A

31692210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952610-G-A

31692210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952610-G-C

31692210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952610-G-T

31692391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952453-G-T

31692421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952433-G-A

31692421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952433-G-T

31692441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952413-T-C

http://identifiers.org/hco/1/GRCh38#31692448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129952406-C-A

31692448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952406-C-T

31692555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952300-C-T

31692669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952198-G-A

31692777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129952119-G-A

31692782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129952114-C-G

31692782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129952114-C-T

31692854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952043-G-A

31692854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129952043-G-T

31692944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951974-T-A

31692952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951973-C-T

http://identifiers.org/hco/1/GRCh38#31692969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951956-C-A

31692969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951956-C-G

31692969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951956-C-T

31693044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951893-G-C

31693044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951893-G-T

31693157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129951781-G-A

31693157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 129951781-G-T

31693207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951741-T-C

http://identifiers.org/hco/1/GRCh38#31693223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951725-C-A

31693223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951725-C-G

http://identifiers.org/hco/1/GRCh38#31693250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951659-C-A

31693250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951659-C-T

http://identifiers.org/hco/1/GRCh38#31693256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951653-A-C

31693256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951653-A-G

http://identifiers.org/hco/1/GRCh38#31693267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951642-A-C

31693287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951622-G-A

31693287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951622-G-T

http://identifiers.org/hco/1/GRCh38#31693358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951554-C-A

31693426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951489-C-T

http://identifiers.org/hco/1/GRCh38#31693467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129951448-C-A

31693633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951234-C-T

31693688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951137-G-A

31693688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129951137-G-C

31693984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950896-C-T

http://identifiers.org/hco/1/GRCh38#31694034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129950862-A-C

31694042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950858-A-G

31694102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950797-G-A

31694102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950797-G-T

http://identifiers.org/hco/1/GRCh38#31694220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129950686-C-A

31694220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950686-C-T

31694221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950685-A-G

31694221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950685-A-T

31694247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950659-A-G

http://identifiers.org/hco/1/GRCh38#31694277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129950636-C-A

31694277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950636-C-T

http://identifiers.org/hco/1/GRCh38#31694321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129950600-A-C

31694560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950372-G-A

31694602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950352-C-T

http://identifiers.org/hco/1/GRCh38#31694811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129950171-C-A

http://identifiers.org/hco/1/GRCh38#31694925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129950059-C-A

31694971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129950005-A-G

31695064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949918-A-G

31695086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949896-G-T

http://identifiers.org/hco/1/GRCh38#31695089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129949893-C-A

31695089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949893-C-G

31695193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129949809-T-C

http://identifiers.org/hco/1/GRCh38#31695288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129949707-C-A

31695288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949707-C-T

http://identifiers.org/hco/1/GRCh38#31695292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129949703-A-C

http://identifiers.org/hco/1/GRCh38#31695294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129949701-C-A

31695713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949347-G-A

31695713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949347-G-T

31695734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949326-C-T

31695737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949324-C-T

http://identifiers.org/hco/1/GRCh38#31695970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129949090-C-A

31695970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129949090-C-T

http://identifiers.org/hco/1/GRCh38#31696072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129948998-C-A

31696072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948998-C-T

31696125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129948944-G-A

31696125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129948944-G-T

31696179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948912-G-A

31696179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948912-G-T

31696246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948844-A-G

http://identifiers.org/hco/1/GRCh38#31696373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129948732-A-C

31696373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948732-A-G

31696502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948603-G-A

31696739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948448-C-T

31696884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948314-G-T

31696885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948313-C-T

31696897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948301-A-G

31696982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129948246-T-A

31697210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129948027-G-C

31697420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947819-G-A

31697420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947819-G-T

31697520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947618-G-T

31697567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947587-T-C

31697567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947587-T-G

31697603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947551-C-G

31697603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947551-C-T

http://identifiers.org/hco/1/GRCh38#31697735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129947436-A-C

31697776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947395-T-A

31697776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129947395-T-G

31697976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129947241-G-A

31697976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129947241-G-C

31698002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 129947215-G-A

31698003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129947214-C-T

31698039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129947178-A-T

31698127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129947090-C-T

31698333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946907-G-A

31698333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946907-G-C

31698333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946907-G-T

31698340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946900-G-A

31698340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946900-G-T

31698349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946892-G-A

31698349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946892-G-C

31698349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946892-G-T

31698355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946886-G-A

31698355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946886-G-T

31698384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946862-A-G

http://identifiers.org/hco/1/GRCh38#31698445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129946804-A-C

31698445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946804-A-G

31698701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946593-A-G

31698717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129946579-C-T

31698764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129946541-T-C

31698765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 129946540-T-C

31699679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945832-A-T

31699732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945791-G-A

31699732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945791-G-T

31700002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945548-G-T

31700046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 129945515-A-T

31700128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945433-G-A

31700179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945387-G-A

31700179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945387-G-T

http://identifiers.org/hco/1/GRCh38#31700218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129945348-C-A

31700218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945348-C-T

31700221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945345-T-A

31700221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129945345-T-C

31700769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944863-A-G

31700865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944773-G-A

31700886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944751-G-A

http://identifiers.org/hco/1/GRCh38#31700947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129944702-C-A

31700947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944702-C-T

http://identifiers.org/hco/1/GRCh38#31701065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129944572-A-C

31701310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944336-G-C

http://identifiers.org/hco/1/GRCh38#31701359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129944282-C-A

31701359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129944282-C-G

31701361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129944280-T-C

31701367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129944277-G-C

31701369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129944275-G-A

http://identifiers.org/hco/1/GRCh38#31701377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#129944267-C-A

31701377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 129944267-C-T

31701574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944038-C-T

31701601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944012-G-A

31701602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129944011-G-C

31701848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943784-G-A

http://identifiers.org/hco/1/GRCh38#31701974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129943655-C-A

31701974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943655-C-G

31701974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943655-C-T

http://identifiers.org/hco/1/GRCh38#31702292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129943372-C-A

31702305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943363-G-T

31702311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943355-G-T

http://identifiers.org/hco/1/GRCh38#31702317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129943349-C-A

31702317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943349-C-T

http://identifiers.org/hco/1/GRCh38#31702338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129943333-C-A

31702338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943333-C-G

31702338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943333-C-T

31702341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943330-G-A

31702341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129943330-G-T

31703272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129942460-C-T

31703293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129942450-T-C

31703485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 129942225-G-C

31703839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 129941872-G-A

31704018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129941665-G-A

31704018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 129941665-G-T

31704144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5 prime UTR variant
orthologous variants: 129941544-A-G

31704157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5 prime UTR variant
orthologous variants: 129941531-G-T

http://identifiers.org/hco/1/GRCh38#31704182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#129941507-C-A

31704200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5 prime UTR variant
orthologous variants: 129941489-G-A

31704200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5 prime UTR variant
orthologous variants: 129941489-G-T

31704298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2193
most severe consequence: 5 prime UTR variant
orthologous variants: 129941385-T-C