108910200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114164248-G-T

http://identifiers.org/hco/12/GRCh38#108910378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114164402-C-A

108910471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114164531-G-T

108910738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114164891-G-A

108910889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165030-C-G

http://identifiers.org/hco/12/GRCh38#108910921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165066-C-A

108910921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165066-C-T

108910922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165067-A-G

108911009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165154-T-C

http://identifiers.org/hco/12/GRCh38#108911042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165185-A-C

108911042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165185-A-G

108911203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165310-G-A

108911203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165310-G-T

108911230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165334-T-C

http://identifiers.org/hco/12/GRCh38#108911710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165489-A-C

108911710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165489-A-G

http://identifiers.org/hco/12/GRCh38#108911727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165506-A-C

108911727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165506-A-G

108911732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165511-G-T

108911813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165563-G-A

108911813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165563-G-C

108911813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165563-G-T

http://identifiers.org/hco/12/GRCh38#108911894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165654-C-A

108911894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165654-C-T

108911997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 114165753-T-A

108911997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 114165753-T-C

108912145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114165929-T-A

http://identifiers.org/hco/12/GRCh38#108912156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165940-C-A

http://identifiers.org/hco/12/GRCh38#108912163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114165947-C-A

108912243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114166027-G-T

108912256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114166041-G-T

http://identifiers.org/hco/12/GRCh38#108912305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114166088-C-A

http://identifiers.org/hco/12/GRCh38#108912422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114166212-C-A

108912422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114166212-C-T

108912429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114166219-T-G

http://identifiers.org/hco/12/GRCh38#108912461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114166260-C-A

108912461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3 prime UTR variant
orthologous variants: 114166260-C-T

108915691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114168105-A-G

http://identifiers.org/hco/12/GRCh38#108915708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114168120-C-A

108915708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114168120-C-T

108915795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: synonymous variant
orthologous variants: 114168170-C-T

108915828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: synonymous variant
orthologous variants: 114168203-G-A

108915893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114168270-A-G

108915930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114168308-A-G

http://identifiers.org/hco/12/GRCh38#108915939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114168317-C-A

108915939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114168317-C-T

108916067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114168394-G-A

108917990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169566-G-A

108917990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169566-G-C

108917990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169566-G-T

http://identifiers.org/hco/12/GRCh38#108917998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114169574-C-A

108917998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169574-C-T

108918012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169591-T-C

108918012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169591-T-G

108918235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169815-C-T

108918246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169830-T-C

108918439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114169983-G-A

108918755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170261-T-C

108919820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170908-C-T

108919872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170945-T-C

108919872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170945-T-G

108919877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170950-T-G

108919883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170956-G-A

108919883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114170956-G-T

108920200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114171026-G-A

108920314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114171157-T-C

108920398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114171234-T-C

108920399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114171235-G-A

108920595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114171478-T-A

108920595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114171478-T-C

108922802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 114173326-G-T

108922817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114173341-A-T

108922838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114173364-G-A

108934008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176445-T-G

108934010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176447-G-C

108934033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176465-G-A

108934033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176465-G-T

108934038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176470-A-T

http://identifiers.org/hco/12/GRCh38#108934094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114176508-A-C

108934094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176508-A-G

108934094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176508-A-T

108934117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176531-G-A

108934117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176531-G-T

108934129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176543-T-C

http://identifiers.org/hco/12/GRCh38#108934169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114176573-C-A

108934169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176573-C-G

108934169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114176573-C-T

108935522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114178679-C-T

108935523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114178680-A-G

http://identifiers.org/hco/12/GRCh38#108935588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114178746-C-A

108935618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114178776-C-T

108935770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114178956-A-G

108935797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114178993-G-A

108935855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114179034-C-T

108935910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114179078-A-G

108938726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114180172-C-G

http://identifiers.org/hco/12/GRCh38#108938740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114180186-C-A

108938740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114180186-C-T

108938745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114180191-G-A

http://identifiers.org/hco/12/GRCh38#108938768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114180208-C-A

108938969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180391-G-T

108939065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180491-G-A

108939159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180552-C-G

108939159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180552-C-T

108940750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180835-C-G

108940750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180835-C-T

108940751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: intron variant
orthologous variants: 114180836-A-G

108940889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 114180972-T-C

108940967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114181045-T-C

108940967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114181045-T-G

108940979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114181056-T-C

108940986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114181063-A-G

108940987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114181064-A-G

108945023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114183550-T-C

108945024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114183551-T-C

108945024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114183551-T-G

108945033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114183560-G-A

108945033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114183560-G-T

108945058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114183585-C-T

108945683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114184132-G-A

108945791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114184245-G-A

108946055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114184545-C-G

108946091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114184581-G-T

http://identifiers.org/hco/12/GRCh38#108951318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114184883-C-A

108953495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114186643-G-C

108955366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114190410-G-A

108955408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114190450-C-T

108955441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114190483-G-C

108955518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114190582-C-T

108960991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 114192606-C-T

108961012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 114192627-A-G

108961033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 114192648-G-A

108961050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 114192665-G-A

http://identifiers.org/hco/12/GRCh38#108961088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114192701-C-A

108966285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114194664-T-C

108966305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114194692-G-T

108966479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114194827-A-G

108966528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114194866-A-G

108966528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114194866-A-T

108966614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114194949-G-A

108966679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114195028-C-T

108966686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114195035-C-T

108966923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114195178-A-G

108966991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114195251-A-G

108967076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114195322-A-T

108972417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 114198131-G-A

108977305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114200998-G-A

108977332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114201021-T-C

108977333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114201022-A-G

108977382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114201070-C-T

108977410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114201098-T-A

108977410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114201098-T-C

108977440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114201128-G-A

108977440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 114201128-G-T

108977443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 114201131-A-G

108977974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114202321-G-A

http://identifiers.org/hco/12/GRCh38#108978030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114202371-C-A

108978091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114202430-T-C

108978375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114202742-G-T

http://identifiers.org/hco/12/GRCh38#108978380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114202746-C-A

108978381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114202747-T-C

108978381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 114202747-T-G

108978451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114202808-T-A

108978486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114202843-G-T

http://identifiers.org/hco/12/GRCh38#108978489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114202848-C-A

108978492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114202851-T-C

http://identifiers.org/hco/12/GRCh38#108978500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114202858-C-A

108978590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114202941-A-G

108978590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114202941-A-T

108978713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203065-T-C

108978721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203073-G-C

108978724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203076-T-C

108983347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203415-C-T

108983386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203439-C-G

108983476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203512-G-A

108983476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203512-G-T

108983488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203524-G-T

108983510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203546-G-A

108983510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203546-G-T

http://identifiers.org/hco/12/GRCh38#108983587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114203572-C-A

108983587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203572-C-T

108983635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114203621-T-C

108983704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114203690-T-C

108983713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114203699-G-T

108983731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114203717-A-G

108983770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114203756-C-G

108983784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114203770-T-C

http://identifiers.org/hco/12/GRCh38#108983802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114203788-C-A

108983802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114203788-C-T

108983825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114203811-G-T

http://identifiers.org/hco/12/GRCh38#108983836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114203822-C-A

108983836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114203822-C-T

108983844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 114203830-G-A

108983844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 114203830-G-T

108983868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203853-G-T

108983886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203871-G-A

108983886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114203871-G-T

108984731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114204762-C-T

108984756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114204787-C-T

108986049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114205459-A-G

108986124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114205529-A-G

108986200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114205599-C-T

108986280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114205675-C-G

108986365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114205755-A-G

108986438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114205828-T-G

http://identifiers.org/hco/12/GRCh38#108990721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114209749-A-C

108990938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114209881-T-C

108990960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114209900-T-C

108991017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114209953-G-A

108991034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114209971-A-G

108991085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114210022-C-G

108991096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114210033-C-T

108991122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114210057-C-T

108991174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114210110-G-A

109009206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114219342-C-T

109009210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114219346-C-T

http://identifiers.org/hco/12/GRCh38#109009300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114219427-A-C

109009318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114219438-C-G

109009322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114219442-C-G

109009322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114219442-C-T

109009404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114219523-G-A

109018008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114225588-G-A

109018254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114225933-C-T

109018296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114225969-C-G

109019314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114227828-T-C

109019456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114227946-T-G

109019486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114227976-A-T

109019660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114228133-G-A

109019660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114228133-G-C

109020527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114228921-T-A

109020629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114229033-A-G

http://identifiers.org/hco/12/GRCh38#109020717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114229110-C-A

109020717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114229110-C-G

109020717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114229110-C-T

http://identifiers.org/hco/12/GRCh38#109020745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114229137-C-A

109020745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114229137-C-G

109020745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 114229137-C-T

http://identifiers.org/hco/12/GRCh38#109020931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114229307-C-A

109020931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114229307-C-T

109020971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114229344-G-A

109020971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114229344-G-T

109020972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114229345-C-T

http://identifiers.org/hco/12/GRCh38#109020981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114229354-C-A

109020981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114229354-C-T

http://identifiers.org/hco/12/GRCh38#109021027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114229391-C-A

109021027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114229391-C-G

109021060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114229429-G-A

109021060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25417
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114229429-G-T