25861846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53369695-A-T

25862027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53369852-A-G

25862058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53369883-G-C

25862058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53369883-G-T

http://identifiers.org/hco/4/GRCh38#25862150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53369976-C-A

25862150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53369976-C-G

25862150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53369976-C-T

http://identifiers.org/hco/4/GRCh38#25862224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370050-C-A

25862224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370050-C-T

25862231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370057-C-T

http://identifiers.org/hco/4/GRCh38#25862296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370118-C-A

25862296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370118-C-G

25862296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370118-C-T

25862306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370128-G-A

25862306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370128-G-C

25862306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370128-G-T

25862352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370169-G-A

http://identifiers.org/hco/4/GRCh38#25862384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370199-C-A

25862388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370203-G-A

http://identifiers.org/hco/4/GRCh38#25862418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370233-C-A

25862608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370407-G-A

25862608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370407-G-C

25862608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370407-G-T

http://identifiers.org/hco/4/GRCh38#25862627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370425-C-A

25862627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370425-C-T

25862742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53370542-G-A

25862742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53370542-G-C

25862742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53370542-G-T

http://identifiers.org/hco/4/GRCh38#25862897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370709-C-A

25862897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53370709-C-G

25862897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53370709-C-T

25862924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370736-G-A

25862924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370736-G-C

25862924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370736-G-T

25862946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370757-G-A

25862946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370757-G-C

25862946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370757-G-T

http://identifiers.org/hco/4/GRCh38#25862952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370763-A-C

25862952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370763-A-G

http://identifiers.org/hco/4/GRCh38#25863049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#53370861-C-A

25863049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53370861-C-T

25863169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53370979-C-G

25863197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371009-C-G

25863197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371009-C-T

http://identifiers.org/hco/4/GRCh38#25863209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53371021-C-A

http://identifiers.org/hco/4/GRCh38#25863285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53371096-C-A

25863285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371096-C-T

http://identifiers.org/hco/4/GRCh38#25863339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#53371111-A-C

25863339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371111-A-G

http://identifiers.org/hco/4/GRCh38#25863421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#53371198-C-A

25863421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371198-C-G

25863421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371198-C-T

25863507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 53371306-C-G

25863507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 53371306-C-T

http://identifiers.org/hco/4/GRCh38#25863635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#53371435-C-A

25863635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371435-C-G

25863635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371435-C-T

http://identifiers.org/hco/4/GRCh38#25863682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#53371483-C-A

25863682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371483-C-T

25863753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371551-C-G

25863753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53371551-C-T

25863773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371571-C-T

25863853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53371649-T-A

25864209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372010-G-A

25864209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372010-G-C

25864871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53372783-C-T

http://identifiers.org/hco/4/GRCh38#25864940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53372870-C-A

25864940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53372870-C-T

http://identifiers.org/hco/4/GRCh38#25864953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53372883-C-A

25864975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53372904-T-A

25865039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53372966-C-T

25865103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373019-T-C

25865160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373077-G-A

25865160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373077-G-T

25865163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373080-G-T

25865192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373111-G-A

25865192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373111-G-T

25865309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373203-A-G

25865381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373284-G-C

25865381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53373284-G-T

25865421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53373322-G-C

25865771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53373672-A-G

http://identifiers.org/hco/4/GRCh38#25867100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53375277-C-A

25867196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53375356-G-A

25867288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53375419-C-T

25867730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53375779-C-G

25867759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53375796-T-C

25868986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53376604-A-G

25869064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53376683-A-T

http://identifiers.org/hco/4/GRCh38#25869186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53376799-C-A

25869196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53376809-G-C

http://identifiers.org/hco/4/GRCh38#25869281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53376895-C-A

25869321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53376970-A-G

25869347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53376995-G-T

http://identifiers.org/hco/4/GRCh38#25869497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53377147-C-A

25869497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53377147-C-T

http://identifiers.org/hco/4/GRCh38#25869555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53377329-C-A

25869700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53377472-G-A

25870602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378517-C-G

25870602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378517-C-T

http://identifiers.org/hco/4/GRCh38#25870627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53378542-A-C

25870631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53378546-C-T

http://identifiers.org/hco/4/GRCh38#25871055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53378965-C-A

25872797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380160-G-A

25872834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380197-T-G

25872854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380217-G-A

25872912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380282-C-T

25873004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380320-T-C

25873392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380597-A-T

25873571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380761-G-C

25873734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380963-A-G

25873742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53380971-T-C

25873954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381178-C-T

25873989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381210-A-T

25874003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381224-G-A

25874014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381235-C-T

25874017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381238-C-T

25874303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381493-A-G

25874327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381507-A-G

25874344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381524-A-T

25874398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381578-G-A

25874435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381615-T-C

25874462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381640-T-C

25874488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381666-G-A

25874544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381722-T-C

25874779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381957-C-G

25874779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53381957-C-T

http://identifiers.org/hco/4/GRCh38#25874878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53382051-A-C

25874878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382051-A-T

25875455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382847-G-A

25875470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382862-T-G

25875533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53382925-A-G

25876150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383881-A-T

25876188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53383938-T-G

25876468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384200-T-C

25876583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384292-T-C

25876747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384455-T-A

25876748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384456-G-A

25877205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53384874-T-C

25878091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53385691-C-T

25878174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53385769-C-T

25878175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53385770-G-A

25878574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53386205-T-G

25879505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53388145-G-A

http://identifiers.org/hco/4/GRCh38#25879964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53388543-C-A

25880098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53388673-G-T

25880343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53389106-C-T

25880542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53389280-G-T

25881739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53391175-G-A

http://identifiers.org/hco/4/GRCh38#25881769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53391202-C-A

25881769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53391202-C-G

25881793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53391226-A-T

http://identifiers.org/hco/4/GRCh38#25881850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53391283-C-A

25881850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53391283-C-T

25882123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53391678-G-A

25882430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53392122-G-A

25882434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53392126-T-C

25882446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53392138-G-T

25883609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53392665-T-C

25883960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53392987-G-T

25884127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53393110-G-A

http://identifiers.org/hco/4/GRCh38#25884128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53393111-C-A

25884268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53393244-T-C

25884998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53394153-G-T

25885286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53394442-C-G

25885292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53394448-T-G

25885425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53394585-G-C

25885816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53394832-G-A

25885935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53394946-C-T

25886170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53395162-T-C

25886290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53395335-C-T

25888826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53396190-T-C

25889704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397048-T-G

25889918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397221-C-T

25890061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397359-G-C

25890099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397389-T-G

25890509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397782-C-T

25890632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397909-T-A

25890632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53397909-T-C

25890741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53398023-G-A

25890803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53398085-C-T

25890976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53398356-C-T

http://identifiers.org/hco/4/GRCh38#25891165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53398514-A-C

25891215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53398563-C-T

http://identifiers.org/hco/4/GRCh38#25891519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53398856-C-A

25891602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53398957-C-T

http://identifiers.org/hco/4/GRCh38#25892168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53399523-A-C

25892350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53399708-C-T

25893187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53400553-C-T

25893258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53400623-G-A

25893667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53401067-C-T

25893668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53401068-G-A

http://identifiers.org/hco/4/GRCh38#25893708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53401107-C-A

25894641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53401989-G-A

25894641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53401989-G-T

25894697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53402045-A-G

25894751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53402108-C-T

25895206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53402717-T-C

25895628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53403087-G-A

25895660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53403119-T-C

25895672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53403133-A-G

25895758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53403204-C-G

25896231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53404526-T-A

25897016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53404943-G-A

25897016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53404943-G-T

25899851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405230-A-G

25900155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405490-T-G

25900245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405564-T-G

25900267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405586-A-T

25900440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405763-A-G

25900512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405849-A-G

25900569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405900-C-T

25900658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53405985-A-G

25901282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53406939-C-T

25901309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53406966-G-A

http://identifiers.org/hco/4/GRCh38#25901327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53406984-C-A

25901447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53407097-C-T

25902033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53407670-G-A

25902252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53407860-G-T

http://identifiers.org/hco/4/GRCh38#25902272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53407876-C-A

25902272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53407876-C-T

25902688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53408322-T-C

25902729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53408363-T-A

25904235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53408872-A-G

25904373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53409013-A-G

25904644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53409282-T-C

25904691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53409327-G-A

25904872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53409498-G-A

http://identifiers.org/hco/4/GRCh38#25905173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53409807-A-C

http://identifiers.org/hco/4/GRCh38#25907213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53412441-C-A

25907388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53412611-A-G

25907484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53412674-C-T

http://identifiers.org/hco/4/GRCh38#25907530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53412748-C-A

25907530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53412748-C-T

25907541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53412759-G-A

25907541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53412759-G-C

25907726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53412949-A-G

25907791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413009-G-A

25907902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413133-G-A

http://identifiers.org/hco/4/GRCh38#25908015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413310-A-C

25908032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413327-T-C

http://identifiers.org/hco/4/GRCh38#25908040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413335-C-A

25908042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413337-C-G

http://identifiers.org/hco/4/GRCh38#25908052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413347-A-C

25908052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413347-A-G

http://identifiers.org/hco/4/GRCh38#25908066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413361-C-A

25908066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413361-C-T

25908068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413363-A-G

http://identifiers.org/hco/4/GRCh38#25908070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413365-C-A

http://identifiers.org/hco/4/GRCh38#25908072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413367-A-C

25908072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413367-A-T

http://identifiers.org/hco/4/GRCh38#25908074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53413369-A-C

25908108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53413406-T-C

25908316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53413735-A-G

25908729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53414112-G-A

25908843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414233-G-T

25908871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53414261-A-G

25909757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415453-T-G

25909816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415511-A-G

25909816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415511-A-T

25909856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415551-G-A

25910248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53415930-T-C

25910775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53419694-T-C

25911045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53419941-C-T

25911078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53419972-T-C

25911204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53420134-T-C

25911289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53420218-G-T

25911296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53420225-G-T

25911534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53420831-G-A

25911578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53420873-C-T

25912700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423039-T-C

25912837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53423159-C-T

25912969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53423278-T-C

25913013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53423321-T-C

25913051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53423363-G-A

25913081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423393-G-A

25913084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423396-T-C

25913387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423696-G-A

25913430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423750-T-C

25913589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423963-C-T

25913590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53423964-G-C

25913718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424090-C-T

25913802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424162-G-T

25913982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424276-G-A

25914044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53424334-A-G

25914044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53424334-A-T

25914088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53424381-T-C

25914088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53424381-T-G

25914204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424479-G-A

25914204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424479-G-C

http://identifiers.org/hco/4/GRCh38#25914222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53424497-C-A

25914222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424497-C-G

25914231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424506-G-A

25914231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424506-G-C

25914231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424506-G-T

25914234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424509-G-A

25914234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424509-G-T

25914251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424526-G-A

25914251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424526-G-C

25914251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424526-G-T

25914258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424533-T-C

25914258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424533-T-G

25914259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424534-G-T

25914266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424541-G-A

25914266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424541-G-C

25914266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424541-G-T

25914268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424543-G-T

http://identifiers.org/hco/4/GRCh38#25914278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53424554-C-A

25914278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424554-C-T

25914309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53424583-A-G

25914483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424773-T-C

25914483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424773-T-G

25914531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424817-G-C

25914531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424817-G-T

25914570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424856-G-A

25914570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424856-G-T

25914624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424907-G-A

25914645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53424925-A-G

25914796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425077-G-A

25914997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425226-C-T

25915050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425279-A-T

25915436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425658-C-T

25915457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425672-G-A

25915457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425672-G-C

25915483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425698-G-A

25915511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425726-G-A

25915513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425728-G-A

25915604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425822-T-A

25915604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425822-T-C

25915751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53425968-G-C

http://identifiers.org/hco/4/GRCh38#25915837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53426031-C-A

25915837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426031-C-T

25915842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426036-C-T

25915851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426045-G-T

25915857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426051-G-C

25915857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426051-G-T

http://identifiers.org/hco/4/GRCh38#25915882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53426073-A-C

25915882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426073-A-G

25915882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426073-A-T

25916038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53426160-T-C

http://identifiers.org/hco/4/GRCh38#25922776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53429859-C-A

25923495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53430584-A-G

25923758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53430827-T-C

25923787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53430856-A-G

25923875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53430945-A-G

25923960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431089-A-G

25924020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431188-C-T

25924021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431189-G-A

25924032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431208-T-G

25924118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431302-G-T

25924781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431940-A-G

25924781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53431940-A-T

25926158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53432504-A-G

http://identifiers.org/hco/4/GRCh38#25926680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53433020-C-A

25926864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433183-G-A

25926917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433235-G-A

25926917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433235-G-T

http://identifiers.org/hco/4/GRCh38#25926924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53433242-C-A

25926924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433242-C-T

25927385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433637-G-A

25927385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433637-G-C

25927552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53433783-T-C

25928073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434289-G-A

25928073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434289-G-T

http://identifiers.org/hco/4/GRCh38#25928270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53434438-C-A

25928270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53434438-C-T

25928345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53434517-G-A

25928345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53434517-G-T

25928388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434556-A-G

http://identifiers.org/hco/4/GRCh38#25928396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53434561-C-A

25928396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434561-C-T

25928441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434590-G-A

25928441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434590-G-T

25928546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434684-C-T

25928585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434723-G-A

25928585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434723-G-T

25928601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434739-C-T

25928719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434843-T-C

25928747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53434864-G-T

25929009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53435085-G-T

http://identifiers.org/hco/4/GRCh38#25929026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53435103-C-A

25929026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53435103-C-T

http://identifiers.org/hco/4/GRCh38#25929232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#53435314-C-A

25929232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435314-C-T

25929303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435382-G-A

25929303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435382-G-C

25929303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435382-G-T

25929381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435455-A-G

25929510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435572-G-A

25929514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435576-G-C

25929514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53435576-G-T

25929705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3 prime UTR variant
orthologous variants: 53435790-G-A

25929705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37260
most severe consequence: 3 prime UTR variant
orthologous variants: 53435790-G-T