38472819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 158251771-T-C

38472893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 158251848-G-A

38472893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 158251848-G-T

http://identifiers.org/hco/20/GRCh38#38472909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158251865-C-A

38472909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5 prime UTR variant
orthologous variants: 158251865-C-G

38472909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5 prime UTR variant
orthologous variants: 158251865-C-T

38473116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158252088-T-C

38473322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158252264-G-A

38473812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158252724-T-G

http://identifiers.org/hco/20/GRCh38#38474057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158253090-C-A

38474251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158253281-T-G

38475102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158253960-A-G

38475242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158254090-C-G

38475245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158254093-G-A

38475298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158254130-G-A

38475887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158254984-G-A

38475974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158255130-T-C

38476097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158255253-T-C

38476217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158255378-T-C

38476238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158255399-A-T

38476994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158255880-G-C

38477069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158255948-A-G

38477363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158256144-G-T

38477503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158256287-T-C

38479447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158257246-A-G

38486735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158260360-C-G

38486735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158260360-C-T

38486763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158260388-T-C

38486767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158260392-T-A

38487164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158260717-C-G

38487378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158260990-T-G

38488378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158262709-A-G

38488378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158262709-A-T

http://identifiers.org/hco/20/GRCh38#38488514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158262845-A-C

38488514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense variant
orthologous variants: 158262845-A-G

38488626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 158262957-T-C

38488813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158263315-C-T

38488857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158263361-G-C

38489100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158263941-C-T

38489171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158264013-G-T

38489420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158264048-G-C

38489610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158264206-A-G

38489673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158264246-G-T

38489751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158265005-C-T

38489812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158265061-T-C

38491092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158266019-C-G

38491322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158266316-A-T

38491323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158266317-C-T

38491658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158266876-G-T

38492053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158267287-A-G

38492405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158267595-C-T

http://identifiers.org/hco/20/GRCh38#38492614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158267787-C-A

38492869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158268022-A-T

http://identifiers.org/hco/20/GRCh38#38493178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158268335-A-C

38493178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158268335-A-G

http://identifiers.org/hco/20/GRCh38#38493189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158268350-A-C

38493259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158268408-G-A

38493259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158268408-G-T

38493272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158268421-T-C

38493282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158268428-G-A

38495040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158269422-G-A

38495298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158269670-A-T

38495607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158270133-G-A

38495796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 158270288-C-G

38495796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 158270288-C-T

38496060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158270737-G-A

38496316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158271455-T-C

38496496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158271595-G-A

38496672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158271728-A-G

38496714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158271766-G-T

http://identifiers.org/hco/20/GRCh38#38496818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158271840-A-C

38496871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158271870-A-G

38497208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158272201-T-A

38497208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158272201-T-C

38497258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158272244-T-C

38497594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158272573-T-C

38497594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158272573-T-G

38498029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158273117-A-G

38498046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158273143-G-A

http://identifiers.org/hco/20/GRCh38#38498061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158273176-C-A

38498264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158273534-A-G

38498319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158273589-G-A

38498319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158273589-G-C

38498629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158273889-C-G

38499221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158274448-G-A

38499271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158274501-G-T

http://identifiers.org/hco/20/GRCh38#38509254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158277524-C-A

38509254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277524-C-G

38509254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277524-C-T

38509273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277543-T-C

http://identifiers.org/hco/20/GRCh38#38509304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158277569-A-C

38509304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277569-A-G

http://identifiers.org/hco/20/GRCh38#38509320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158277585-A-C

38509320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277585-A-G

http://identifiers.org/hco/20/GRCh38#38509336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158277602-C-A

38509336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277602-C-T

http://identifiers.org/hco/20/GRCh38#38509348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158277614-C-A

38509348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277614-C-G

38509348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158277614-C-T

http://identifiers.org/hco/20/GRCh38#38509355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158277621-C-A

http://identifiers.org/hco/20/GRCh38#38516115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158278022-C-A

38516145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158278055-A-G

38516152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158278371-T-C

38516291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158278509-G-A

38516291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158278509-G-C

38516396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158278615-G-A

38516458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158278671-G-A

38516458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158278671-G-T

38516495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158278708-G-A

38517585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158279002-T-A

38517746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158279142-T-G

38517912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158279308-C-T

38518122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158279511-A-G

38518164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158279554-T-A

38518261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158279651-T-A

38518355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158279745-A-T

38518382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158279779-A-G

38518699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158280045-A-G

38518825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158280168-C-G

38518893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158280225-T-G

38519035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158280321-G-A

38519035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158280321-G-T

38519080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158280371-G-C

38520212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158281421-G-T

38520334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158281544-T-G

http://identifiers.org/hco/20/GRCh38#38520502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158281714-C-A

38521634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158282827-A-G

38521645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158282838-G-A

38521806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158282999-T-C

38522022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158283206-G-A

38522042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158283226-G-A

38522294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158283453-C-T

38523546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158284444-A-G

38523693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158284516-T-C

38524394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158284901-C-G

38525024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285404-T-G

http://identifiers.org/hco/20/GRCh38#38525095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158285473-C-A

38525095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285473-C-T

38525105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285483-C-T

38525171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285548-G-A

38525267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285618-T-C

38525318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285663-T-C

38525318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158285663-T-G

38526085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158286694-G-A

38526140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158286743-T-C

38531058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158287811-G-A

38531058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158287811-G-T

http://identifiers.org/hco/20/GRCh38#38531252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158288132-C-A

38531299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158288179-A-G

38531865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158289170-A-G

http://identifiers.org/hco/20/GRCh38#38532641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158290137-C-A

http://identifiers.org/hco/20/GRCh38#38533001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158290525-C-A

38533075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158290581-G-A

38533088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158290594-A-G

38533088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158290594-A-T

38533239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158290704-G-T

38533292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158290756-T-C

38533319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158290780-A-G

38534929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291954-G-T

38534933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291958-T-C

38534933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291958-T-G

38534941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291966-G-A

38534941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291966-G-T

38534948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291973-T-C

38534949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291974-G-A

38534949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158291974-G-T

38535222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158292241-C-T

http://identifiers.org/hco/20/GRCh38#38535256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158292275-C-A

38535256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158292275-C-G

38535264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158292283-T-C

38536151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158292807-C-G

38536268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158292940-G-T

38536730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158293361-G-A

38536753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158293384-T-G

38537180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 158293774-A-G

38538823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 158294937-A-G

38538873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158295041-A-G

http://identifiers.org/hco/20/GRCh38#38538952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158295247-A-C

38538976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158295264-C-G

38538976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158295264-C-T

38539001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158295290-T-C

38539205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158295486-A-G

http://identifiers.org/hco/20/GRCh38#38539703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158295978-C-A

38540000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158296264-T-C

38540393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158297073-G-C

38540971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158298111-T-C

38540971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158298111-T-G

38541763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158299045-T-C

38543836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158300764-G-A

38543840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158300768-T-G

38543878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158300801-G-C

38543916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158300838-A-T

http://identifiers.org/hco/20/GRCh38#38544158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158301002-C-A

38544459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158301293-T-C

38546069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158303831-G-A

http://identifiers.org/hco/20/GRCh38#38546131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158303884-C-A

38546131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158303884-C-T

38546148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158303901-A-G

38546156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158303907-G-C

38546473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304222-T-G

http://identifiers.org/hco/20/GRCh38#38546577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158304315-A-C

38546599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304335-T-C

http://identifiers.org/hco/20/GRCh38#38546722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158304476-C-A

38546722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304476-C-T

38546785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304539-A-G

38546874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304623-G-T

38547326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304888-A-G

http://identifiers.org/hco/20/GRCh38#38547454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158304953-C-A

38547477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304971-T-C

38547501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158304995-C-T

38547574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158305060-G-T

38547683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158305134-G-T

38547685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158305136-T-C

http://identifiers.org/hco/20/GRCh38#38548027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158305479-A-C

38548027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158305479-A-G

38548191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305619-A-G

38548217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305645-C-G

38548217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305645-C-T

http://identifiers.org/hco/20/GRCh38#38548233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158305659-C-A

38548233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305659-C-T

38548297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305723-C-T

38548523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305854-A-G

38548527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305858-G-A

38548557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305871-G-T

38548594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305896-G-T

38548611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158305913-G-T

38548892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158306234-G-T

38548916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158306258-G-A

38548916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158306258-G-T

38549038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158306377-A-T

38549217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158306527-T-C

http://identifiers.org/hco/20/GRCh38#38550962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158307615-A-C

38550964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158307617-A-G

38551040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158307703-G-A

38551298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158307967-G-A

38551355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308019-G-A

38551355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308019-G-T

38553163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308227-A-G

38553221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308286-G-T

38553234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308297-G-C

38553289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308327-C-T

38553415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308416-A-G

38553545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308502-A-G

38553945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense variant
orthologous variants: 158308734-G-A

38553945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense variant
orthologous variants: 158308734-G-C

38554058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: synonymous variant
orthologous variants: 158308847-G-A

38554084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 158308873-T-G

38554156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308955-G-A

38554156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158308955-G-T

http://identifiers.org/hco/20/GRCh38#38554205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158309002-A-C

38554205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158309002-A-G

38554222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158309018-T-A

38554257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158309055-A-G

38554293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158309068-G-C

38555742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158311736-C-T

38555985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158311973-A-G

http://identifiers.org/hco/20/GRCh38#38556068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158312045-A-C

38556381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158312327-G-A

38556547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158312446-G-T

38556617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158312521-G-A

38556732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158312865-T-G

38557030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158313310-A-G

38557443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158313905-T-A

38557614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158314086-G-A

38557804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158314231-T-G

38557902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158314343-G-T

38558230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158314988-G-T

38558354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: synonymous variant
orthologous variants: 158315102-A-G

38558477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158315225-T-C

http://identifiers.org/hco/20/GRCh38#38558503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158315245-C-A

38561420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158316067-T-C

38561550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158316167-G-A

http://identifiers.org/hco/20/GRCh38#38561678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158316328-A-C

38562263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158317784-G-A

38562265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158317786-A-G

38562436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158317932-G-A

38562436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158317932-G-T

38562514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158318007-G-A

38562576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: missense variant
orthologous variants: 158318069-C-G

38562728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158318217-G-T

38562731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158318220-T-C

38564135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, undefined
orthologous variants: 158318805-A-G

http://identifiers.org/hco/20/GRCh38#38564451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158319093-A-C

38564750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158319344-A-G

38565494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158319700-C-T

38565504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158319710-T-A

http://identifiers.org/hco/20/GRCh38#38565622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158319826-A-C

38565622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158319826-A-G

38565622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158319826-A-T

38565672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158322321-T-C

38565818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158322451-C-T

38565975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158322600-A-G

38566169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158322971-G-C

38566276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158323074-G-C

38566701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158323687-A-G

38566968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158324170-G-A

38566968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158324170-G-C

38566968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158324170-G-T

38567297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158324484-G-A

38567297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron variant
orthologous variants: 158324484-G-T

38568527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158326540-G-A

38568527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158326540-G-T

38568639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158326647-A-G

38568803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158326807-T-C

http://identifiers.org/hco/20/GRCh38#38568925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158326930-C-A

38569252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158327193-C-T

38569346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158327286-G-T

38569764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158334171-A-G

38569764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 158334171-A-T

38569890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 158334286-C-T

38570012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158334414-T-A

http://identifiers.org/hco/20/GRCh38#38570135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158334506-C-A

38570414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158334551-G-A

38570596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158334732-G-A

38570617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158334752-A-G

http://identifiers.org/hco/20/GRCh38#38570731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158334824-A-C

38570908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158334994-T-A

38573725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336184-C-T

http://identifiers.org/hco/20/GRCh38#38573798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158336234-C-A

38573854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336285-C-T

38573879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336309-T-C

38573979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336408-G-T

38573991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336420-G-A

38573991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336420-G-T

http://identifiers.org/hco/20/GRCh38#38574036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158336452-C-A

38574036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336452-C-T

http://identifiers.org/hco/20/GRCh38#38574069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158336478-A-C

38574069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336478-A-G

http://identifiers.org/hco/20/GRCh38#38574081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158336485-C-A

38574081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158336485-C-G

38574258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 158336653-C-G

38574258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 158336653-C-T

38574375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158337022-A-G

38574565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158337196-A-T

38574745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 158337345-C-T

38575441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338009-A-G

38575468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338034-C-T

38575482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338045-G-A

38575482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338045-G-T

38575660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338209-G-A

http://identifiers.org/hco/20/GRCh38#38575727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158338272-C-A

38575727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338272-C-T

38575732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338277-C-T

http://identifiers.org/hco/20/GRCh38#38575739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158338283-C-A

38575739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 158338283-C-T

38575880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158338396-C-T

38576016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158338518-G-A

38576097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158338568-T-A

38576126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158338598-G-A

http://identifiers.org/hco/20/GRCh38#38576170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158338645-C-A

38576401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158338851-G-T

38576824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158339296-A-G

http://identifiers.org/hco/20/GRCh38#38577034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158339511-C-A

http://identifiers.org/hco/20/GRCh38#38577102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158339583-C-A

38577102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158339583-C-T

38577114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158339595-G-T

38577120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158339600-C-G

http://identifiers.org/hco/20/GRCh38#38577121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158339601-C-A

38577167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158339635-A-G

http://identifiers.org/hco/20/GRCh38#38577205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158339673-A-C

38577373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158339838-A-G

http://identifiers.org/hco/20/GRCh38#38577574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158340037-C-A

38577574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158340037-C-T

http://identifiers.org/hco/20/GRCh38#38577624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158340058-C-A

38577708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158340148-C-T

38577825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158340250-A-T

http://identifiers.org/hco/20/GRCh38#38577836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158340262-C-A

38577836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 158340262-C-T

38578722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3 prime UTR variant
orthologous variants: 158341036-T-C

http://identifiers.org/hco/20/GRCh38#38578753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29221
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#158341067-C-A