52316094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron variant
orthologous variants: 31048140-C-T

52316335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31047912-A-G

52316347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31047900-A-G

52316378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31047890-A-G

52316389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31047879-G-T

52316587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047705-G-T

52317151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047158-T-A

52317151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31047158-T-G

52317789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045932-T-C

52317803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045918-C-T

http://identifiers.org/hco/3/GRCh38#52317846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31045876-C-A

52317849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045872-A-G

52317870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045851-G-T

52317922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045799-G-A

52317922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045799-G-T

52317961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045769-G-A

52317961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045769-G-T

52317975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045756-G-A

52318048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045740-T-C

52318682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31045342-A-G

52318751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045275-T-C

52318894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31045124-G-T

http://identifiers.org/hco/3/GRCh38#52319552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31044537-C-A

52319552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044537-C-T

http://identifiers.org/hco/3/GRCh38#52319696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31044391-C-A

52319696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044391-C-T

52319728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044381-C-T

52319927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31044238-G-A

52320401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043766-C-T

52320479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043694-T-C

52320540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043630-G-C

52320661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31043503-C-T

52321400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042897-G-A

52321445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042855-G-A

http://identifiers.org/hco/3/GRCh38#52321455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31042845-A-C

52321469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042831-T-A

http://identifiers.org/hco/3/GRCh38#52321504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31042797-C-A

52321559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042741-G-T

52321574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042725-A-G

52321698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31042609-G-A

52321746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 31042561-G-T

52321820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042487-G-T

http://identifiers.org/hco/3/GRCh38#52321837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31042470-C-A

52321842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042465-T-A

52321868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042439-G-T

52321992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042342-G-T

52322100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042242-G-A

52322100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042242-G-T

52322290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042127-T-C

52322304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042113-G-A

52322304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042113-G-T

http://identifiers.org/hco/3/GRCh38#52322342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31042066-C-A

52322342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042066-C-T

52322376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042031-C-T

52322386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31042021-C-G

52322592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31041842-A-G

52322788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041667-G-A

52322858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041601-A-G

52322858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041601-A-T

52322862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041597-A-T

52322863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041596-G-A

52322863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041596-G-T

http://identifiers.org/hco/3/GRCh38#52322869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31041590-C-A

52322869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041590-C-G

http://identifiers.org/hco/3/GRCh38#52323241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31041278-A-C

52323334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041190-G-A

52323499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041019-T-A

52323499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31041019-T-C

52323548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040970-G-A

52323699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040868-G-A

http://identifiers.org/hco/3/GRCh38#52323791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31040852-C-A

52323791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040852-C-T

52323897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040748-G-A

52323897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040748-G-T

52323898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040747-C-G

52323898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040747-C-T

52323919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040728-G-A

52323919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040728-G-C

52323919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040728-G-T

52323968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040681-T-C

52324002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040647-A-G

52324224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040457-T-C

52324279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040429-T-G

52324323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040389-C-T

52324348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040365-G-C

52324491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040289-T-C

52324546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040236-G-T

52324660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040107-T-C

52324661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040106-G-A

52324661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040106-G-T

52324677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040090-A-T

52324678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040089-T-C

52324757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040019-G-A

52324757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31040019-G-C

52325685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039113-T-C

http://identifiers.org/hco/3/GRCh38#52325739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31039069-A-C

52325739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039069-A-G

52325791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31039013-T-A

52325992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038872-T-C

52326045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038821-A-G

52326045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038821-A-T

52326074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038784-G-T

http://identifiers.org/hco/3/GRCh38#52326107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31038748-C-A

52326107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038748-C-T

52326111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038745-G-T

52326125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038731-T-A

http://identifiers.org/hco/3/GRCh38#52326386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31038467-C-A

52326557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038304-A-G

52326591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038269-A-G

52326631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038255-G-A

52326631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038255-G-T

http://identifiers.org/hco/3/GRCh38#52326633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31038253-C-A

52326633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31038253-C-T

52326753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31038206-G-A

52326811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31038148-C-T

http://identifiers.org/hco/3/GRCh38#52327040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31037930-C-A

52327158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037804-A-G

52327268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037703-T-C

http://identifiers.org/hco/3/GRCh38#52327365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31037605-A-C

52327409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037564-G-A

52327448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037518-G-A

52327472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037494-C-T

52327660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31037307-A-G

http://identifiers.org/hco/3/GRCh38#52327858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31037172-C-A

52327966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31037065-C-T

52328108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036925-G-A

52328108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036925-G-C

52328108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036925-G-T

52328143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036889-A-G

52328283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036280-A-T

52328284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036279-T-C

52328459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036149-T-C

52328532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31036095-C-T

52328644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31035977-C-T

http://identifiers.org/hco/3/GRCh38#52328672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31035949-C-A

52329468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31035183-G-A

52330890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033991-G-A

52330893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033988-G-T

52331015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033877-G-A

52331015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033877-G-C

52331015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033877-G-T

http://identifiers.org/hco/3/GRCh38#52331068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31033824-C-A

52331068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033824-C-T

http://identifiers.org/hco/3/GRCh38#52331099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31033793-C-A

52331099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033793-C-T

http://identifiers.org/hco/3/GRCh38#52331100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31033792-C-A

52331100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033792-C-T

52331195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31033696-G-A

52331216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31033675-A-G

http://identifiers.org/hco/3/GRCh38#52331261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31033630-C-A

52331261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31033630-C-G

52331261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 31033630-C-T

52331283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31033608-T-C

52331295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31033596-G-C

http://identifiers.org/hco/3/GRCh38#52331379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31033527-C-A

http://identifiers.org/hco/3/GRCh38#52331407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31033510-C-A

52331407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033510-C-T

52332017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033164-G-T

52332019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033162-T-A

52332019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033162-T-G

52332089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033095-C-T

52332109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033075-T-C

52332123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31033061-C-T

52332309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31032876-G-A

http://identifiers.org/hco/3/GRCh38#52344467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31030932-C-A

52344702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030715-C-T

52344712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030705-T-A

52344712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030705-T-C

52344791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030619-T-C

52344873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030545-G-A

52344873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030545-G-C

52344977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030438-A-G

52345036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030352-T-C

52345083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030291-G-A

52345085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030289-A-G

52345086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030288-C-T

http://identifiers.org/hco/3/GRCh38#52345347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31030046-A-C

52345347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31030046-A-G

http://identifiers.org/hco/3/GRCh38#52345423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31029974-C-A

http://identifiers.org/hco/3/GRCh38#52345480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31029913-C-A

52345480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029913-C-T

52345732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029666-G-A

http://identifiers.org/hco/3/GRCh38#52345751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31029650-C-A

52345751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029650-C-G

52345751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029650-C-T

http://identifiers.org/hco/3/GRCh38#52345769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31029632-A-C

52346010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029482-A-G

52346145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31029391-G-T

http://identifiers.org/hco/3/GRCh38#52346434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31029153-C-A

52346722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31028865-G-T

52346789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028799-G-T

52346816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028783-G-A

52346816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028783-G-T

52346856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028747-A-G

52347068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028560-A-G

52347119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028513-G-A

52347271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028394-G-C

52347338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028328-A-T

52347382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028285-G-A

52347440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028249-C-T

52347458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028230-G-T

52347473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028211-T-C

52347543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028146-G-A

52347607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028114-G-A

52347710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028004-G-A

52347710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31028004-G-T

http://identifiers.org/hco/3/GRCh38#52347811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31027935-C-A

52347811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027935-C-T

http://identifiers.org/hco/3/GRCh38#52347837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31027908-C-A

52347837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31027908-C-G

52347837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31027908-C-T

52347897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31027848-G-C

52347897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 31027848-G-T

52347900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 31027845-C-T

52347992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027753-A-G

http://identifiers.org/hco/3/GRCh38#52348082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31027619-C-A

52348082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027619-C-G

52348082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027619-C-T

52348129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027572-A-T

52348411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027367-G-A

http://identifiers.org/hco/3/GRCh38#52348457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31027323-A-C

52348569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027209-A-G

http://identifiers.org/hco/3/GRCh38#52348798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31027043-C-A

52348798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31027043-C-T

http://identifiers.org/hco/3/GRCh38#52348810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31027031-A-C

http://identifiers.org/hco/3/GRCh38#52349056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31026791-A-C

52349238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31026576-G-A

52349238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31026576-G-T

52349620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31026215-G-C

52349936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025914-G-A

52349936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025914-G-T

52349979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025871-C-T

52349981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31025870-A-G

52350055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31025796-G-T

52350124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025727-G-A

52350124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025727-G-T

52350138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025704-G-A

52350138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025704-G-T

52350149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025688-G-T

52350153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025682-G-A

52350154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025681-G-A

52350154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025681-G-C

52350154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025681-G-T

http://identifiers.org/hco/3/GRCh38#52350168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31025647-A-C

52350168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025647-A-T

52350199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025616-G-T

52350239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025578-G-C

52350239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025578-G-T

52350423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025386-A-G

52350461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025351-C-T

52350469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025343-T-A

52350469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025343-T-C

52350535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31025285-T-C

52350604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025216-T-C

52350641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025179-A-G

52350725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025097-A-T

52350733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31025089-G-T

52351807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024570-G-A

http://identifiers.org/hco/3/GRCh38#52351877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31024471-C-A

52351877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024471-C-T

52351879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024469-T-C

52352059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31024294-A-G

52352218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31024174-G-T

52352406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023982-G-A

http://identifiers.org/hco/3/GRCh38#52352505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31023903-C-A

52352505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023903-C-G

52352505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023903-C-T

http://identifiers.org/hco/3/GRCh38#52352739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31023678-C-A

52352739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023678-C-T

http://identifiers.org/hco/3/GRCh38#52352786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31023632-C-A

52352786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023632-C-T

http://identifiers.org/hco/3/GRCh38#52352791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31023627-C-A

52352803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023615-G-C

52352803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023615-G-T

http://identifiers.org/hco/3/GRCh38#52352851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31023570-C-A

52352851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023570-C-T

52353020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023405-G-T

52353062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023363-T-A

52353062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023363-T-C

52353070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31023357-G-A

52353097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31023337-C-G

52353336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022997-G-A

http://identifiers.org/hco/3/GRCh38#52353574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022758-C-A

52353647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022681-A-G

http://identifiers.org/hco/3/GRCh38#52353706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022618-C-A

52353706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022618-C-T

52353727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022597-A-G

52353727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022597-A-T

http://identifiers.org/hco/3/GRCh38#52353728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022596-C-A

52353728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022596-C-G

52353728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022596-C-T

52353802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31022545-A-G

http://identifiers.org/hco/3/GRCh38#52353803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022544-C-A

http://identifiers.org/hco/3/GRCh38#52353843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022503-C-A

http://identifiers.org/hco/3/GRCh38#52353878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022470-A-C

http://identifiers.org/hco/3/GRCh38#52353888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022460-C-A

52353888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022460-C-T

http://identifiers.org/hco/3/GRCh38#52354728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31022178-C-A

52354728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022178-C-T

52354745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022161-T-C

52354750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022156-A-G

52354819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022089-A-G

52354834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022073-C-G

52354834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31022073-C-T

52354852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31022055-A-G

http://identifiers.org/hco/3/GRCh38#52354993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31021914-C-A

52354993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31021914-C-T

http://identifiers.org/hco/3/GRCh38#52355111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31021808-C-A

52355111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021808-C-G

52355111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021808-C-T

52355291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021656-G-T

52355435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021553-C-T

52355686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021333-G-A

52355877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021132-C-G

52356008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021008-G-T

52356015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31021001-C-T

52356022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020992-C-T

52356547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020780-T-C

52356572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020747-G-A

52356572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020747-G-T

52356573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020746-A-G

52356573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020746-A-T

52356576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020743-G-A

52356576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020743-G-T

52356922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020416-G-C

52357395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020340-G-A

52357470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020270-A-T

52357482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020258-A-G

52357493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020247-G-A

52357493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020247-G-T

52357509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020230-G-T

http://identifiers.org/hco/3/GRCh38#52357523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31020225-C-A

52357523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020225-C-T

52357568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020174-G-A

52357568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020174-G-T

52357570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31020172-A-T

52357737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 31020000-T-C

52357737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 31020000-T-G

52357754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019984-T-C

52357779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019278-C-T

52357798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019251-G-T

52357807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019242-A-G

52357807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019242-A-T

52357811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31019238-T-C

52358076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018980-T-A

52358076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018980-T-C

52358118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018940-G-C

52358118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018940-G-T

52358331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018769-A-G

52358436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018701-G-A

52358436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018701-G-T

52358498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018641-G-A

http://identifiers.org/hco/3/GRCh38#52358531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31018613-C-A

52358531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018613-C-T

52358615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018528-G-C

52358675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018468-G-A

52358795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018360-G-A

52359267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018272-C-G

52359267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31018272-C-T

http://identifiers.org/hco/3/GRCh38#52359276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31018263-C-A

52359276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018263-C-T

52359292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018247-T-C

52359327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018212-G-A

52359327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31018212-G-T

52359483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31018083-G-T

52359578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017991-C-T

52359600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017969-G-T

52359652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017921-G-T

52359734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017842-G-A

52359751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017825-A-G

52359793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017783-T-C

http://identifiers.org/hco/3/GRCh38#52359825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31017751-C-A

52359825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017751-C-T

52359863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017711-G-A

52360188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017402-G-A

52360188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017402-G-T

52360236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017354-C-G

http://identifiers.org/hco/3/GRCh38#52360260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31017331-C-A

52360260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017331-C-T

52360291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017300-T-A

52360300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017291-T-C

http://identifiers.org/hco/3/GRCh38#52360327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31017264-A-C

52360327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31017264-A-G

52360430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017161-C-T

52360938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017114-T-C

52360941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017111-C-T

52360995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017057-C-T

http://identifiers.org/hco/3/GRCh38#52361021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31017026-C-A

52361021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017026-C-T

http://identifiers.org/hco/3/GRCh38#52361022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31017025-C-A

52361024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017023-G-T

52361030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31017017-G-A

52361065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016984-G-A

52361065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016984-G-T

52361107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016928-A-T

52361136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016901-C-T

52361379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016669-G-A

52361379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016669-G-T

52361442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016621-G-A

52361442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016621-G-T

http://identifiers.org/hco/3/GRCh38#52361444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31016619-C-A

52361444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016619-C-G

52361480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016593-G-T

52361494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016573-G-A

52361494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016573-G-T

http://identifiers.org/hco/3/GRCh38#52361610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31016464-A-C

52361610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016464-A-G

52361627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016449-C-T

http://identifiers.org/hco/3/GRCh38#52361826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31016259-C-A

52361826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016259-C-T

52361842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016252-G-A

52361842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016252-G-T

http://identifiers.org/hco/3/GRCh38#52361862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31016235-C-A

52361862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016235-C-G

http://identifiers.org/hco/3/GRCh38#52361906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31016211-C-A

52361906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016211-C-T

http://identifiers.org/hco/3/GRCh38#52361955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31016183-C-A

52361957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016181-C-T

52362130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016014-G-A

52362130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31016014-G-T

http://identifiers.org/hco/3/GRCh38#52362244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31015896-A-C

52362244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015896-A-G

52362277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015864-T-C

http://identifiers.org/hco/3/GRCh38#52362301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31015841-C-A

52362301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015841-C-T

http://identifiers.org/hco/3/GRCh38#52362349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31015803-C-A

52362349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015803-C-G

52362349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015803-C-T

52362549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015599-G-T

52362565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015583-A-G

http://identifiers.org/hco/3/GRCh38#52362582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31015566-C-A

52362602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015540-G-T

52362607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015535-G-A

52362607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015535-G-T

52362609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015533-G-A

52362609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015533-G-T

52362908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015233-G-C

52362951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015182-G-A

52362951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31015182-G-T

http://identifiers.org/hco/3/GRCh38#52364502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31014792-C-A

52364527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014767-T-A

52364527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014767-T-C

http://identifiers.org/hco/3/GRCh38#52364740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31014560-C-A

52364740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014560-C-G

52364740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014560-C-T

52364743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014557-G-A

52364743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014557-G-T

52364787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014501-G-C

52364805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014485-C-T

52364896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31014392-A-G

52364908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31014380-G-A

52365051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014215-G-T

52365116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014151-G-A

52365116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014151-G-T

52365155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014124-T-C

52365257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31014022-T-A

52365465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013757-C-T

52365640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013560-C-G

52365666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013534-G-C

52365869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013352-C-G

52365952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013262-C-T

52366094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013164-T-G

52366219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31013048-C-T

52366317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012948-G-T

52366322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012943-C-T

52366328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012937-C-G

52366328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012937-C-T

52366361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012904-G-A

52366392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012873-G-A

52366392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012873-G-T

52366404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012861-G-A

52366404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012861-G-T

http://identifiers.org/hco/3/GRCh38#52366412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31012853-C-A

52366436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012829-G-A

52366436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012829-G-T

52366617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012659-G-A

52366617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012659-G-T

52366643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012630-G-A

52366643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012630-G-T

52366673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012597-C-G

http://identifiers.org/hco/3/GRCh38#52366901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31012362-C-A

52366901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012362-C-G

52366901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012362-C-T

52366920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012345-C-T

52367015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012281-T-C

52367111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012199-A-G

52367221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31012066-G-C

52367454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31011821-T-C

52368645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009936-G-A

52368645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009936-G-T

52368748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31009837-G-A

52368748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31009837-G-C

52368748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31009837-G-T

52368928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009658-C-T

52368934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009652-C-T

52369201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009450-C-T

52369629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009075-C-G

52369632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009072-A-G

http://identifiers.org/hco/3/GRCh38#52369677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31009027-C-A

52369679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009025-T-A

52369679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31009025-T-C

http://identifiers.org/hco/3/GRCh38#52369723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008975-C-A

52369723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008975-C-G

http://identifiers.org/hco/3/GRCh38#52369725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008973-C-A

52369725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008973-C-G

52369725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008973-C-T

http://identifiers.org/hco/3/GRCh38#52369773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008924-C-A

52369825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 31008872-G-C

52369956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31008741-G-A

http://identifiers.org/hco/3/GRCh38#52370103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008592-C-A

52370103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31008592-C-T

52370312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008393-A-G

52370346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008370-A-G

http://identifiers.org/hco/3/GRCh38#52370349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008367-C-A

52370349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008367-C-T

http://identifiers.org/hco/3/GRCh38#52370436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008312-C-A

52370454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008304-G-T

http://identifiers.org/hco/3/GRCh38#52370458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31008300-C-A

52370458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008300-C-T

52370656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31008088-G-A

52370793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31007956-G-A

52370799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 31007950-G-T

52370814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31007935-G-A

52370814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 31007935-G-T

http://identifiers.org/hco/3/GRCh38#52370830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31007919-C-A

52370830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007919-C-T

52370836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007913-G-T

52370907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007838-A-G

52370960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007786-A-G

52371235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007495-A-G

52371262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007469-C-T

52371523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007246-C-T

52371636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007135-C-T

52371667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007107-C-T

52371711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007054-T-G

52371712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31007053-G-A

52371798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006965-T-C

52371873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006898-G-T

52371885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006886-G-A

52371885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006886-G-C

52371885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006886-G-T

52372106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006671-C-T

52372121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006657-C-T

52372178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006596-C-G

52372178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006596-C-T

52372179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006595-T-A

52372198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006576-A-G

52372198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006576-A-T

52372217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006561-G-A

52372217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006561-G-C

52372218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006560-C-T

52372245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31006533-A-G

http://identifiers.org/hco/3/GRCh38#52372260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31006518-A-C

52372260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31006518-A-T

http://identifiers.org/hco/3/GRCh38#52372396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31006382-C-A

http://identifiers.org/hco/3/GRCh38#52372413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31006365-A-C

52372451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006349-T-C

52372455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006345-A-G

52372501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006298-G-C

52372501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006298-G-T

http://identifiers.org/hco/3/GRCh38#52372514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31006285-C-A

52372514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006285-C-T

http://identifiers.org/hco/3/GRCh38#52372518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31006281-C-A

52372518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006281-C-G

52372518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006281-C-T

52372522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006277-T-A

52372522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006277-T-C

52372728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006109-C-T

52372871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31006017-G-A

52372948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005941-G-A

52372948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005941-G-C

52373060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31005829-G-A

52373129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005761-G-A

52373129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005761-G-T

http://identifiers.org/hco/3/GRCh38#52375287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31005263-C-A

52375287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005263-C-G

http://identifiers.org/hco/3/GRCh38#52375290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31005260-C-A

52375290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005260-C-G

52375344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005206-C-G

52375351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005199-T-A

52375353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005197-G-A

52375353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005197-G-C

52375353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31005197-G-T

52375427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005123-G-A

52375427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005123-G-T

52375487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005065-G-T

52375488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005064-T-A

52375488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005064-T-C

52375514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31005039-A-G

52375556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004995-G-A

52375556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004995-G-T

52375695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004850-G-A

http://identifiers.org/hco/3/GRCh38#52375702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31004843-A-C

52375834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004721-T-C

http://identifiers.org/hco/3/GRCh38#52375886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31004479-A-C

52376033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004325-G-A

52376076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004276-A-G

52376183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004190-A-G

52376280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004094-C-T

52376331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004028-G-A

52376331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004028-G-T

52376338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004024-G-A

52376348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004010-C-T

52376357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31004001-C-T

52376495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003843-C-G

http://identifiers.org/hco/3/GRCh38#52376598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31003732-C-A

52376598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003732-C-T

52376627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003704-C-T

52376641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31003689-C-T

52376980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002788-T-A

52377005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002763-C-G

52377084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002686-G-A

52377588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002181-G-A

52377588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31002181-G-C

52377783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001961-G-A

52378100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001681-C-T

52378180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001604-T-G

52378337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001463-C-T

52378373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001416-A-G

http://identifiers.org/hco/3/GRCh38#52378456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#31001310-C-A

52378503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001263-T-A

52378503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001263-T-G

52378504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001262-G-A

52378504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001262-G-C

52378504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001262-G-T

52378507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001259-G-C

52378508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001258-G-A

52378508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001258-G-C

52378508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001258-G-T

52378513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001253-A-G

52378519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31001247-G-A

52378595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31001195-C-T

52378641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31001149-T-C

52378641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31001149-T-G

52378662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31001128-A-G

52378763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31001027-G-A

52379349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000665-G-T

52379545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000499-T-C

52379892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31000169-G-C

52380085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30999977-T-A

52380185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999888-T-C

52380259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999829-G-A

52380259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999829-G-T

52380632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30999447-A-G

52381561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998432-A-G

52381563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998430-G-A

52381584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998403-G-A

52381597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998390-G-A

52381597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998390-G-T

http://identifiers.org/hco/3/GRCh38#52381625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30998285-C-A

52381625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998285-C-G

52381625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998285-C-T

52381852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998065-G-A

52381852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998065-G-T

52381875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998041-G-A

52381875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998041-G-C

52381875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30998041-G-T

52382033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997891-G-T

52382238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997687-A-G

52382245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997669-G-A

52382253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997661-C-G

52382257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997657-C-T

52382458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997456-G-T

http://identifiers.org/hco/3/GRCh38#52382556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30997358-C-A

52382556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997358-C-T

52382558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997356-G-A

52382558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997356-G-C

52382558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997356-G-T

52382770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997164-G-T

52382824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30997118-T-A

http://identifiers.org/hco/3/GRCh38#52383147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30996845-C-A

52383159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30996839-C-G

52383159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30996839-C-T

http://identifiers.org/hco/3/GRCh38#52383304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30996573-C-A

52383304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30996573-C-T

52383470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30996352-G-C

52383470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30996352-G-T

52383640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30996182-T-C

http://identifiers.org/hco/3/GRCh38#52383758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30996100-C-A

http://identifiers.org/hco/3/GRCh38#52383974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30995893-C-A

52383974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30995893-C-G

52383974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30995893-C-T

52384094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995775-G-C

52384094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995775-G-T

http://identifiers.org/hco/3/GRCh38#52384170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30995718-A-C

52384170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995718-A-G

http://identifiers.org/hco/3/GRCh38#52384652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30995108-A-C

52384652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995108-A-G

http://identifiers.org/hco/3/GRCh38#52384755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30995003-C-A

52384755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30995003-C-T

52384836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30994926-G-A

52384995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994768-C-T

52385014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994748-G-C

http://identifiers.org/hco/3/GRCh38#52385045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30994720-C-A

52385045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994720-C-G

52385097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994673-G-T

52385223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30994549-G-A

52385223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30994549-G-T

52385227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30994545-C-T

52385295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30994486-T-C

52385332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 30994394-C-G

52385332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 30994394-C-T

52385353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30994373-A-G

52385511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30994207-G-A

52385511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30994207-G-T

52385948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30993799-C-T

http://identifiers.org/hco/3/GRCh38#52386611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30993169-A-C

http://identifiers.org/hco/3/GRCh38#52386872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30992914-C-A

52386957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992842-T-C

http://identifiers.org/hco/3/GRCh38#52386979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30992820-C-A

52386979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992820-C-G

52386997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992811-A-G

http://identifiers.org/hco/3/GRCh38#52386998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30992810-C-A

52387245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992574-C-T

http://identifiers.org/hco/3/GRCh38#52387711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30992243-A-C

52387731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992222-C-T

52387753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992207-G-A

52387772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30992189-G-C

52388317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30991970-G-A

http://identifiers.org/hco/3/GRCh38#52388342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30991945-C-A

http://identifiers.org/hco/3/GRCh38#52388613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30991677-C-A

52388613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30991677-C-G

52388613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30991677-C-T

52388628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30991664-C-T

52388648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30991642-G-A

52388683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30991586-G-C

52388683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30991586-G-T

http://identifiers.org/hco/3/GRCh38#52388783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30991479-A-C

52389010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30991256-C-T

52389024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30991243-G-A

52389024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30991243-G-T

52389062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30991201-A-G

http://identifiers.org/hco/3/GRCh38#52389335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30990974-A-C

52389419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990904-G-A

52389419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990904-G-T

52389471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30990855-G-A

52389471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30990855-G-T

52389518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30990808-G-A

52389518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30990808-G-T

52389600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990734-G-A

52389600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990734-G-C

52389600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990734-G-T

52389665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990683-T-C

52389673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990675-T-A

52389673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990675-T-C

52389695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990665-A-G

52390763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990227-G-A

52390863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990124-G-A

52390863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30990124-G-T

52390992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30990003-T-C

52391098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989899-A-G

http://identifiers.org/hco/3/GRCh38#52391108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30989880-C-A

52391347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989648-T-A

52391347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989648-T-C

52391348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989647-G-A

http://identifiers.org/hco/3/GRCh38#52391350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30989644-C-A

52391350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989644-C-T

52391359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989634-A-G

52391485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30989528-A-G

http://identifiers.org/hco/3/GRCh38#52391667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30989349-C-A

52391692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989317-T-C

http://identifiers.org/hco/3/GRCh38#52391707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30989304-C-A

52391707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989304-C-T

http://identifiers.org/hco/3/GRCh38#52391718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30989293-C-A

52391718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30989293-C-T

http://identifiers.org/hco/3/GRCh38#52392408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988875-C-A

52392408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988875-C-T

http://identifiers.org/hco/3/GRCh38#52392427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988857-C-A

52392427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988857-C-T

52392430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988854-G-A

52392430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988854-G-C

http://identifiers.org/hco/3/GRCh38#52392712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988572-A-C

52392712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988572-A-G

52392748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988563-T-A

52392748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988563-T-C

52392748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988563-T-G

http://identifiers.org/hco/3/GRCh38#52392778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988533-A-C

http://identifiers.org/hco/3/GRCh38#52392813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988482-A-C

52392813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988482-A-G

52392813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988482-A-T

http://identifiers.org/hco/3/GRCh38#52392815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988480-C-A

52392815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988480-C-T

52392819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988476-T-A

52392819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988476-T-C

52392819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988476-T-G

http://identifiers.org/hco/3/GRCh38#52392820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30988475-A-C

52392820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988475-A-G

52393071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988236-T-C

52393189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988133-G-A

52393189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988133-G-C

52393279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988044-G-A

52393279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30988044-G-C

52393518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30987795-G-A

52393531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30987781-G-T

52393625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30987715-A-G

52394455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30987424-C-T

52394522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30987357-G-T

52394745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30987160-A-G

52394795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30987111-T-C

52394949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30986976-G-A

52394949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30986976-G-C

http://identifiers.org/hco/3/GRCh38#52395075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30986850-C-A

52395075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30986850-C-T

http://identifiers.org/hco/3/GRCh38#52395117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30986825-C-A

52395189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30986759-G-C

52395213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30986737-C-G

52395213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30986737-C-T

http://identifiers.org/hco/3/GRCh38#52395265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30986679-C-A

52395491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30986457-G-A

http://identifiers.org/hco/3/GRCh38#52396362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30985981-C-A

52396362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30985981-C-T

52396374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30985969-A-G

52396374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30985969-A-T

http://identifiers.org/hco/3/GRCh38#52396455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30985888-A-C

52396455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30985888-A-G

52396937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30985181-A-G

52396937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30985181-A-T

52397092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30985041-G-A

52397092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30985041-G-T

52397135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984991-T-C

52397185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984953-T-G

52397200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984930-C-G

52397232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984896-G-A

52397320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984832-C-T

52397487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984706-G-A

52397528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984672-G-A

52397528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984672-G-C

52397568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984638-G-T

52397678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984568-G-A

52397678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984568-G-C

52398020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984250-T-C

52398026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30984244-C-G

52398068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30984202-G-T

52398072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30984198-C-G

http://identifiers.org/hco/3/GRCh38#52398182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30984089-C-A

52398182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984089-C-T

52398211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30984060-T-C

52398758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983859-T-C

52398779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983846-T-G

52398947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30983698-G-A

52398950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30983695-G-C

http://identifiers.org/hco/3/GRCh38#52399399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30983355-C-A

52399437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983323-G-A

52399437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983323-G-T

52399480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983295-T-C

52399480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983295-T-G

52399481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30983294-G-T

http://identifiers.org/hco/3/GRCh38#52399540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30983240-C-A

52399552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30983228-T-C

52399680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30983100-A-G

52399799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30982979-A-G

52399853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30982944-A-G

52400210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30982632-G-A

52400210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30982632-G-T

http://identifiers.org/hco/3/GRCh38#52400218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30982624-C-A

52400218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2940
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30982624-C-T