223857661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659575-T-C

223857729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659656-C-T

223857786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659713-C-T

223857880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659797-C-T

223857961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659865-A-G

223858049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659995-G-A

223858049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79659995-G-T

223859562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79660544-C-T

223859586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79660564-T-G

223859631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79660609-G-C

223859771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79660732-C-G

223860200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79660856-T-G

223860787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79662419-T-C

223861305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79662625-G-C

223861305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79662625-G-T

223861388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79662709-A-G

223861829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79663126-G-A

223861891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79663175-T-C

223861925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79663219-C-T

223862018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79663346-G-A

223862073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79663389-A-T

223863520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79670728-T-A

223863788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79670981-T-A

223863788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79670981-T-C

223863818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79670993-A-G

223863909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79671073-T-C

223863910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79671074-C-T

223863971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79671131-A-G

223864142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79671242-G-A

223864142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79671242-G-C

223869291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79676382-C-G

223869364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79676454-G-A

223871387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79678164-T-C

223875203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79679846-G-T

223875291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79679928-C-T

223875336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79679972-A-G

223875408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680066-G-A

223875408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680066-G-C

http://identifiers.org/hco/2/GRCh38#223875443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79680099-C-A

223875604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680267-T-C

223876031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680659-T-A

223876031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680659-T-C

223876118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680749-T-C

223876145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680776-C-T

223876200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680827-G-T

223876234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79680861-G-T

223876428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681037-C-G

223876428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681037-C-T

223876429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681038-T-C

223876466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681065-G-A

http://identifiers.org/hco/2/GRCh38#223876735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79681307-C-A

223876735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681307-C-T

223876855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681397-C-T

223877009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681545-G-T

223877026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681562-T-C

223877041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681577-C-G

223877145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681673-G-A

http://identifiers.org/hco/2/GRCh38#223877262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79681936-C-A

http://identifiers.org/hco/2/GRCh38#223877280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79681951-C-A

http://identifiers.org/hco/2/GRCh38#223877322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79681983-A-C

223877322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79681983-A-T

223877363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682024-T-A

223877388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682048-G-A

223877409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682079-T-C

http://identifiers.org/hco/2/GRCh38#223877828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79682444-C-A

http://identifiers.org/hco/2/GRCh38#223877971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79682582-C-A

223877971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682582-C-T

223878011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682597-A-G

223878165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682746-T-C

223878316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682879-T-G

223878321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79682884-A-G

http://identifiers.org/hco/2/GRCh38#223878463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79683023-C-A

223878463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79683023-C-T

223878638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79683191-G-C

223878638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79683191-G-T

223878645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79683199-G-A

223878745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79683302-G-T

223878752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79683304-A-G

http://identifiers.org/hco/2/GRCh38#223879994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79683836-C-A

223879994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79683836-C-G

223880016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79683858-T-C

223880016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79683858-T-G

223880255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684089-T-C

223880267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684100-T-C

223880536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684233-G-A

http://identifiers.org/hco/2/GRCh38#223880984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79684472-A-C

223881070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684525-G-C

http://identifiers.org/hco/2/GRCh38#223881096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79684551-C-A

223881096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684551-C-T

223881393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684758-C-G

223881455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79684824-A-G

223881911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79685140-G-C

223882465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79685351-G-A

223882503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79685384-A-G

223882665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79685539-C-T

223883420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79685837-T-G

223883423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79685840-C-T

http://identifiers.org/hco/2/GRCh38#223884149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79686402-A-C

223884552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79686706-G-A

223884552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79686706-G-T

223884590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79686751-G-C

223884590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79686751-G-T

223884630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79686792-T-G

223884684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79686846-C-T

223884783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79686946-G-A

http://identifiers.org/hco/2/GRCh38#223884831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79686988-C-A

223889926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79687534-T-C

223890073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79687690-C-T

http://identifiers.org/hco/2/GRCh38#223891515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79688827-C-A

223891591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79688911-G-A

223892956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79689613-A-G

223893746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79690042-C-T

223894180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79691510-G-A

223894180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79691510-G-T

http://identifiers.org/hco/2/GRCh38#223894216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79691544-C-A

223894216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79691544-C-T

223894404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79691739-T-C

223894404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79691739-T-G

223894594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79691893-G-A

223894925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692199-G-T

223895001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692281-A-G

223895192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692445-T-C

223895542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79692629-T-C

223895581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79692668-T-C

223895642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692727-T-A

223895674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692736-A-G

223895674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692736-A-T

223895697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692759-G-A

223895697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692759-G-T

223895708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692770-T-G

223895749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692808-G-A

223895749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692808-G-T

223895768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692825-G-A

223895768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79692825-G-T

http://identifiers.org/hco/2/GRCh38#223895773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79692830-C-A

223896532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79693409-T-C

223896622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79693489-C-T

223896740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79693608-C-T

223896753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79693621-G-A

223897226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79694095-G-A

223898759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79694733-T-C

223898776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79694750-A-G

223899797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79695307-T-C

223899809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79695331-G-A

223900305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79703239-C-T

http://identifiers.org/hco/2/GRCh38#223900349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79703295-C-A

223900792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79704050-T-A

223900792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79704050-T-C

223900792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79704050-T-G

223900816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79704061-T-A

223900816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79704061-T-C

223900816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron variant
orthologous variants: 79704061-T-G

http://identifiers.org/hco/2/GRCh38#223900950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79704172-C-A

223900950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79704172-C-T

223901080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79704222-T-A

http://identifiers.org/hco/2/GRCh38#223901091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79704233-C-A

http://identifiers.org/hco/2/GRCh38#223901165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79704265-C-A

223901165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79704265-C-T

223901166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79704266-G-A

223901212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79704312-G-A

http://identifiers.org/hco/2/GRCh38#223901295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79704395-C-A

223901371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79704469-A-G

223901405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79704510-C-T

223901445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79704530-G-A

223901445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79704530-G-T

223903143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79706542-T-A

223903143-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79706542-T-G

223903161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79706563-T-C

223905271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79706931-A-T

223905525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707043-T-C

223905829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707252-G-T

http://identifiers.org/hco/2/GRCh38#223905842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79707265-C-A

223905854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707277-T-C

223905862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707285-T-G

223905872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707295-A-G

223905872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707295-A-T

http://identifiers.org/hco/2/GRCh38#223906015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79707441-C-A

223906015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707441-C-T

http://identifiers.org/hco/2/GRCh38#223906017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79707443-C-A

223906017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707443-C-T

223906143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707549-A-G

223906168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707574-G-C

223906402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707804-C-G

223906421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79707819-G-A

http://identifiers.org/hco/2/GRCh38#223906465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79707862-A-C

223910929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79710567-T-C

223911089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79710731-A-G

223911089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79710731-A-T

http://identifiers.org/hco/2/GRCh38#223911141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79710770-A-C

223911141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79710770-A-G

223911179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79710808-G-A

223911610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711230-A-T

http://identifiers.org/hco/2/GRCh38#223911711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79711326-C-A

223911711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711326-C-G

223911711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711326-C-T

http://identifiers.org/hco/2/GRCh38#223911715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79711330-C-A

223911729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711340-T-C

223912379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711643-T-G

223912420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711680-A-T

http://identifiers.org/hco/2/GRCh38#223912431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79711689-C-A

223912431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711689-C-G

223912431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711689-C-T

223912437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711695-G-A

223912437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711695-G-C

223912564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79711825-G-A

223912966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712277-G-A

223913063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712362-G-T

223913066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712365-T-C

223913144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712434-C-T

223913177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712489-G-A

223913205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712516-T-A

223913205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712516-T-C

223913208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712519-A-G

223913209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712520-T-A

223913209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712520-T-C

223913292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79712610-T-C

223914549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714104-G-C

223914561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714118-T-C

223914561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714118-T-G

223914671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714228-A-G

223914686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714243-A-G

223915201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714825-A-T

223915265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79714891-C-T

223915387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79715014-C-G

223915884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79715973-G-C

223915885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79715974-C-T

223915910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79715995-T-C

http://identifiers.org/hco/2/GRCh38#223915973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79716059-C-A

223915986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716072-G-T

223916141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716188-G-A

223916163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716210-G-A

223916217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716251-C-T

223916420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716432-C-T

223916435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716446-C-G

223916435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79716446-C-T

223917062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717257-C-G

223917114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717299-T-G

223917509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717656-G-A

223917509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717656-G-C

223917588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717699-T-C

223917804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717706-C-G

223917804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717706-C-T

223917885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717723-T-C

223917917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717754-T-A

223918049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79717882-G-A

223918791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718737-G-A

http://identifiers.org/hco/2/GRCh38#223918812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79718758-C-A

223918812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718758-C-T

223918823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718769-C-T

http://identifiers.org/hco/2/GRCh38#223918933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79718877-C-A

223918933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718877-C-G

223918933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79718877-C-T

223921143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79719540-T-C

223921344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79719721-A-G

223921459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79719854-G-A

http://identifiers.org/hco/2/GRCh38#223921693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79720141-C-A

223921693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720141-C-T

223921947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720349-C-T

223922195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720580-G-A

223922249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720634-C-T

223922374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720751-C-T

223922487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79720861-C-T

223922665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721023-T-C

223922709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721059-C-G

223922791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721136-C-T

223922818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721163-T-C

223922853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721194-C-G

223922853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721194-C-T

223922921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721268-A-G

http://identifiers.org/hco/2/GRCh38#223923106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79721419-C-A

223923129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721433-G-T

223923252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721565-A-G

223923262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79721575-A-G

223924993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723388-G-C

223925128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723490-T-G

223925136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723497-C-T

223925171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723528-G-A

http://identifiers.org/hco/2/GRCh38#223925175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79723532-C-A

223925175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723532-C-G

http://identifiers.org/hco/2/GRCh38#223928343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79723833-A-C

223928390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723873-G-C

223928390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723873-G-T

http://identifiers.org/hco/2/GRCh38#223928448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79723927-C-A

223928448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723927-C-T

223928494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723956-T-C

223928526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723976-A-G

223928539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79723987-C-T

223928560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79724004-T-G

http://identifiers.org/hco/2/GRCh38#223928614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79724058-A-C

223928906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79724364-G-T

223929151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79724578-C-T

223930123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79726936-C-G

223930273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79727078-T-G

223931195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79727582-C-T

http://identifiers.org/hco/2/GRCh38#223931230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79727617-C-A

223931440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728154-G-T

223931600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728314-T-C

223931606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728320-C-T

223931664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728371-G-A

223932469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728511-G-C

223932536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728570-T-C

223932719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79728744-G-C

http://identifiers.org/hco/2/GRCh38#223932865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79728886-C-A

223933309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79729323-C-G

http://identifiers.org/hco/2/GRCh38#223933336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79729361-A-C

223934460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79729689-A-G

223935048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79729963-A-G

http://identifiers.org/hco/2/GRCh38#223935298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79730262-C-A

223935298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730262-C-T

223935418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730610-A-G

223935681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730860-T-C

223935701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730880-A-G

223935886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79730994-G-A

223935986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731063-G-A

223935986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731063-G-T

http://identifiers.org/hco/2/GRCh38#223936811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79731582-A-C

223936946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79731723-G-C

223937464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79732130-T-C

223939880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735086-C-T

223939916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735123-T-C

223940060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735275-C-T

223940086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79735300-C-T

223940290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736080-T-C

http://identifiers.org/hco/2/GRCh38#223940330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79736119-C-A

223940330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736119-C-G

http://identifiers.org/hco/2/GRCh38#223940371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79736158-C-A

223940488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736268-T-G

223941413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736565-G-A

223941478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736621-T-C

223941482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736625-T-C

223941498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736639-C-T

223941503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736648-A-T

223941505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736650-C-T

223941748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79736962-C-T

223941788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737002-T-C

223941864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79737068-A-T

223941884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737090-G-A

223941884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79737090-G-T

223942055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79737220-T-C

223943228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737460-A-G

223943318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737546-C-T

223943532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737727-C-T

223943570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737764-T-A

223943860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79737996-C-G

223944102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79738259-A-G

223944481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79738621-C-G

223944481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79738621-C-T

223944495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79738633-C-T

223944539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79738678-G-C

223944592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79738721-T-G

http://identifiers.org/hco/2/GRCh38#223944686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79738807-A-C

http://identifiers.org/hco/2/GRCh38#223944713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79738849-C-A

223944802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79738927-C-G

223944802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79738927-C-T

223944810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79738934-G-C

223944810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79738934-G-T

223944924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79739067-G-A

223945041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79739172-T-C

http://identifiers.org/hco/2/GRCh38#223945098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#79739225-C-A

223945098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79739225-C-T

223945208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739341-G-A

223945208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739341-G-T

223945236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79739369-G-A

223945236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739369-G-T

http://identifiers.org/hco/2/GRCh38#223945304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79739428-C-A

223945304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739428-C-T

http://identifiers.org/hco/2/GRCh38#223945308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#79739432-C-A

223945308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739432-C-G

223945308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739432-C-T

223945317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739441-A-G

223945317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20451
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79739441-A-T