35633463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 3 prime UTR variant
orthologous variants: 25019910-T-C

http://identifiers.org/hco/7/GRCh38#35633501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25019952-A-C

35633874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020321-T-C

35633945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020394-T-A

35633945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020394-T-C

35633953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020414-G-A

35633953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020414-G-T

35634032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020488-A-G

35634105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020547-C-T

http://identifiers.org/hco/7/GRCh38#35634220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25020649-A-C

35634256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020681-A-G

35634256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020681-A-T

35634273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020697-T-C

35634273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020697-T-G

http://identifiers.org/hco/7/GRCh38#35634286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25020710-A-C

35634286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25020710-A-G

35634304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 25020728-T-C

35634454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020875-T-A

35634454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020875-T-C

35634483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020893-A-G

35634503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25020910-G-T

35634649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021052-T-C

35634764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021161-T-C

35634764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021161-T-G

35634775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021177-T-C

35634859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021273-C-T

35634892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021466-G-A

35634899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021473-T-C

35634983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25021556-T-G

35635406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25021978-T-C

http://identifiers.org/hco/7/GRCh38#35635505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25022080-C-A

35635505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022080-C-T

35635564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022142-T-C

35635700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022250-G-A

http://identifiers.org/hco/7/GRCh38#35635861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25022369-C-A

35635861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022369-C-T

35635986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25022447-A-G

35636374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25023242-A-G

35636455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25023314-G-A

35637168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25023591-T-A

35637213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25023645-T-G

35637541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25023960-T-C

35637804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024601-T-C

http://identifiers.org/hco/7/GRCh38#35637806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25024602-C-A

35637836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024630-G-A

35637836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024630-G-C

35637928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024731-A-G

35637941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024743-G-A

35637984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024773-T-C

35638001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024789-C-G

http://identifiers.org/hco/7/GRCh38#35638045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25024820-C-A

35638045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024820-C-T

35638230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25024977-A-T

35638281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025072-T-C

35638297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025089-A-G

35638417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 25025184-G-C

35638508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025274-T-C

http://identifiers.org/hco/7/GRCh38#35638511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25025277-C-A

35638517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025283-A-G

35638517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025283-A-T

http://identifiers.org/hco/7/GRCh38#35638549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25025313-C-A

35638553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025317-G-T

35638570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025332-T-A

35638654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025400-G-C

35638667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25025413-T-C

http://identifiers.org/hco/7/GRCh38#35638697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25025415-A-C

35667391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036140-G-T

35667493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25036227-G-C

35667493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 25036227-G-T

35667844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036547-A-G

35667975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036636-G-A

35668240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036876-T-C

http://identifiers.org/hco/7/GRCh38#35668354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25036958-C-A

35668354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036958-C-T

35668355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036959-A-G

35668372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 25036977-T-A

35668763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25037319-C-T

35668838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25037394-A-G

35669243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25037722-T-C

35669891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25041258-G-A

35670183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25041800-G-A

35670183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25041800-G-C

35670183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25041800-G-T

http://identifiers.org/hco/7/GRCh38#35670301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25041918-C-A

35670301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, missense_variant
orthologous variants: 25041918-C-G

35670301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, missense_variant
orthologous variants: 25041918-C-T

http://identifiers.org/hco/7/GRCh38#35670407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25042013-A-C

35670426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042037-T-A

35670426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042037-T-C

35670918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042548-G-A

35670975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042598-C-T

35671370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042902-C-G

35671370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042902-C-T

http://identifiers.org/hco/7/GRCh38#35671422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25042951-C-A

35671422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042951-C-G

35671422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042951-C-T

35671462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25042970-G-A

35671520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25043017-C-T

35671626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25043125-G-A

35671848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25043270-C-T

35671975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25043455-A-G

35672153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25043616-T-C

35672699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044000-T-C

35672720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044014-A-G

http://identifiers.org/hco/7/GRCh38#35672756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25044049-C-A

35672764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044067-G-A

http://identifiers.org/hco/7/GRCh38#35673085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25044406-C-A

35673085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044406-C-T

35673203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 25044493-T-C

35673310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044598-T-A

35673458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044735-G-A

35673503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044799-G-C

35673534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25044859-G-A

35673948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25045362-T-A

http://identifiers.org/hco/7/GRCh38#35673995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25045471-C-A

35674602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25046210-G-A

35674602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25046210-G-C

http://identifiers.org/hco/7/GRCh38#35674604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25046212-C-A

35674727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25046320-T-A

35674727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25046320-T-C

35675119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25046835-G-C

35675323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25046991-C-T

35675334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25047002-T-C

35675474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25047085-A-G

http://identifiers.org/hco/7/GRCh38#35675643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25047225-C-A

35677180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25049840-T-A

35677274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25049929-G-A

35677436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25050088-C-T

35677533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25050242-T-C

35677559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25050268-G-A

35678060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25050791-C-T

35678254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25050944-A-G

35678716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25051077-A-G

35678812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25051175-T-C

35678910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25051252-G-A

35678963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25051300-C-T

35679508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25052682-G-A

http://identifiers.org/hco/7/GRCh38#35679620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25052767-C-A

35679620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25052767-C-T

35679719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25052850-G-A

http://identifiers.org/hco/7/GRCh38#35679745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25052876-A-C

35679984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25053102-T-C

http://identifiers.org/hco/7/GRCh38#35680957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25053865-C-A

35680957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25053865-C-T

35681530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25054362-T-C

35681634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25054451-A-G

35681741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25054540-C-T

35681865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25054638-A-G

35681995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25054763-T-A

http://identifiers.org/hco/7/GRCh38#35685243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25054834-A-C

35686160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25055096-G-A

35687076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25055197-A-G

35687305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25055365-T-G

35687518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25055548-G-A

35687670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25055672-T-G

35687928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25056796-T-C

35688645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25057455-G-T

35689218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25058293-A-G

35689335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25058408-A-G

35689885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25058928-G-A

35690049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25059110-T-C

http://identifiers.org/hco/7/GRCh38#35690181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25059243-A-C

http://identifiers.org/hco/7/GRCh38#35690323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25059379-A-C

http://identifiers.org/hco/7/GRCh38#35690422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25059476-A-C

35690422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25059476-A-G

35690612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25059729-C-G

35691872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25060014-T-A

35692209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25060276-C-T

35692324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25060399-G-C

35692466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25060821-C-T

35692655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25061016-C-T

35692972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25061296-C-T

http://identifiers.org/hco/7/GRCh38#35693367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25061666-A-C

35693367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25061666-A-G

35693538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25061797-G-A

35694144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron variant
orthologous variants: 25062082-T-G

35694361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5 prime UTR variant
orthologous variants: 25062291-G-A

35694361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5 prime UTR variant
orthologous variants: 25062291-G-C

35694361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5 prime UTR variant
orthologous variants: 25062291-G-T

http://identifiers.org/hco/7/GRCh38#35694659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25062538-C-A

35694659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25062538-C-T

http://identifiers.org/hco/7/GRCh38#35694703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25062579-C-A

35694703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25062579-C-T

http://identifiers.org/hco/7/GRCh38#35694827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25062785-C-A

35694827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25062785-C-T

35694849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25062835-A-G

35694852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25062838-G-A

35694852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25062838-G-T

35694886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25062901-G-A

35694886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25062901-G-T

http://identifiers.org/hco/7/GRCh38#35694890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25062903-C-A

http://identifiers.org/hco/7/GRCh38#35694930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25062932-A-C

35694930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 25062932-A-G

35695035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063001-G-A

35695035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063001-G-C

35695035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063001-G-T

35695083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063031-G-A

35695083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063031-G-T

35695091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063039-G-A

35695091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063039-G-T

35695124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063070-G-A

35695124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063070-G-C

35695124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 25063070-G-T

35695144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, undefined
orthologous variants: 25063086-G-T

35695241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063162-T-C

35695245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063166-G-A

35695245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063166-G-C

35695245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063166-G-T

35695279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063191-G-A

35695279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063191-G-T

http://identifiers.org/hco/7/GRCh38#35695280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25063192-C-A

35695280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063192-C-G

35695280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063192-C-T

35695282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063194-G-A

35695282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063194-G-T

35695287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25063199-G-A

35695287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25063199-G-T

http://identifiers.org/hco/7/GRCh38#35695319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#25063207-C-A

35695375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063235-A-G

http://identifiers.org/hco/7/GRCh38#35695431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25063274-C-A

35695431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063274-C-T

http://identifiers.org/hco/7/GRCh38#35695498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#25063345-C-A

35695498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063345-C-T

35695560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063406-T-C

35695605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 25063426-G-C

35695797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25063546-C-T

35696044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 25063786-G-T

35697159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25064205-G-T

35697197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21915
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 25064240-A-G