9641366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32174483-G-T

9641591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32173379-G-T

http://identifiers.org/hco/5/GRCh38#9641598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32173372-C-A

9641811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32173159-G-T

http://identifiers.org/hco/5/GRCh38#9641821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32173149-C-A

9641821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32173149-C-T

9641854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32173113-G-A

9641934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32173033-G-A

http://identifiers.org/hco/5/GRCh38#9641972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32172995-C-A

9642184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32172784-T-C

9642303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32172670-G-A

9642963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32172017-C-T

9644259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32171089-T-A

9644711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170618-C-T

9644759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170581-T-C

9644808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170530-T-C

9644989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170386-A-G

9645000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170375-T-A

9645140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170235-G-A

9645178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170197-G-A

9645290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32170087-G-T

http://identifiers.org/hco/5/GRCh38#9645416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32169989-C-A

9645443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169962-G-A

9645443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169962-G-C

http://identifiers.org/hco/5/GRCh38#9645450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32169955-C-A

9645487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169919-G-A

9645487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169919-G-T

9645493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169913-G-T

9645508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169900-C-T

http://identifiers.org/hco/5/GRCh38#9645510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32169898-C-A

9645542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169864-C-T

9646005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169411-A-G

9646230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32169195-C-T

9646724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32168736-G-A

9646724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32168736-G-T

9646768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32168692-C-T

9647055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32168064-T-G

9647131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32167987-A-G

9647152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32167966-C-T

9647209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32167909-T-C

9647335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32167790-A-G

9647467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32167712-T-C

9647518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32167659-C-G

9648172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32165996-A-G

9648349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32165801-C-T

9648511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32165627-C-T

9649241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32165130-G-A

9649966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32164472-T-A

9649977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32164460-A-T

9649998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32164439-T-C

9650156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32164292-T-C

9650299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32164033-C-G

9650299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32164033-C-T

9650328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163997-T-C

9650343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163941-G-C

9650422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163779-G-A

9650691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163511-C-T

http://identifiers.org/hco/5/GRCh38#9650837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32163382-C-A

9650837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163382-C-T

9650849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163370-G-A

9650856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163363-T-C

9650889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163332-G-A

9651150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32163084-G-A

9651626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162632-A-T

9651686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162562-A-G

9651726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162515-G-A

http://identifiers.org/hco/5/GRCh38#9651735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32162505-A-C

9651735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162505-A-G

9651735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162505-A-T

9651885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162358-G-A

9651940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162288-T-A

9651968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162244-G-C

9652006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162214-T-A

9652043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162179-T-C

9652076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162149-A-G

9652153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162106-C-T

9652199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32162060-G-A

9652450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32161834-T-C

http://identifiers.org/hco/5/GRCh38#9652578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32161710-C-A

9653079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32160328-T-C

9653079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32160328-T-G

9653124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32160285-G-A

9653322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159992-A-G

http://identifiers.org/hco/5/GRCh38#9653390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32159924-C-A

9653592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159739-A-G

9653592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159739-A-T

9653611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159720-C-T

9653635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159696-A-G

9653743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159575-T-C

9653825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159493-C-T

9654164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32159189-C-T

9654494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32157106-T-A

http://identifiers.org/hco/5/GRCh38#9654561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32157091-C-A

9654568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32157084-G-T

9654593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32157058-A-G

9654882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156792-G-A

9654887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156787-G-A

9655076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156600-T-C

9655204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156472-G-T

http://identifiers.org/hco/5/GRCh38#9655246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32156430-A-C

9655572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156124-T-A

9655572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156124-T-C

9655576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156120-A-G

9655624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32156085-G-T

9658162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154433-C-G

9658162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154433-C-T

9658237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154371-G-C

9658237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154371-G-T

9658303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154308-T-A

9658303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154308-T-C

http://identifiers.org/hco/5/GRCh38#9658325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32154290-C-A

9658325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154290-C-G

9658325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154290-C-T

9658334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154281-G-T

9658519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154142-G-A

9658531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154130-G-A

9658531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154130-G-T

9658550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154111-G-A

9658550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154111-G-C

9658550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154111-G-T

9658571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32154096-A-G

http://identifiers.org/hco/5/GRCh38#9658860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32153807-A-C

9658975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153700-T-C

9659278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153431-G-T

9659340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153377-G-T

http://identifiers.org/hco/5/GRCh38#9659369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32153351-C-A

9659369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153351-C-G

9659426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32153293-T-C

http://identifiers.org/hco/5/GRCh38#9659480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#32153240-C-A

9659496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32153224-T-C

http://identifiers.org/hco/5/GRCh38#9659644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32153071-C-A

9659644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153071-C-T

9659645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153070-A-G

9659657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153058-T-C

9660535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150770-T-C

9660570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150748-A-G

9660570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150748-A-T

9660814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150549-C-T

9660863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150499-A-G

9660864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150498-T-A

9660864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150498-T-C

9660942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150424-C-T

9660983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32150388-C-T

http://identifiers.org/hco/5/GRCh38#9661420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32149915-A-C

9661421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32149914-T-C

9661855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32149508-A-G

9661887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32149476-T-C

9661913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32149452-T-G

9661979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32149386-C-G

9662018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32149334-G-A

9662319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32148979-T-G

9662991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141093-G-A

9662998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141086-C-T

http://identifiers.org/hco/5/GRCh38#9663079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32140991-C-A

9663079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140991-C-T

9663869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139729-G-C

9664306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139289-T-C

9664315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139279-C-T

9664412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139139-G-C

9664412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139139-G-T

9665340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32138172-T-G

9665502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32138040-A-G

9665568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137979-C-T

9665601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137948-A-G

9665616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137933-T-C

http://identifiers.org/hco/5/GRCh38#9665776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32137773-A-C

9665880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137674-G-T

9665904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137652-T-C

9666007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137554-T-C

9666128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137439-A-G

9666129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137438-A-G

9666253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137302-A-G

9666460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137114-G-A

http://identifiers.org/hco/5/GRCh38#9673360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32135974-A-C

9673419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135925-T-C

9673521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135816-T-C

9673675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135635-G-A

9673675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135635-G-T

9673740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135570-A-G

9673802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135525-C-T

9673953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135454-T-C

9674100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32135432-T-C

9681157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32133768-C-T

9681239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32133684-T-C

9681239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32133684-T-G

http://identifiers.org/hco/5/GRCh38#9681560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32133374-C-A

9681615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32133294-T-A

9681619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32133290-T-G

http://identifiers.org/hco/5/GRCh38#9681840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32133079-A-C

9682023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132879-T-A

9682083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132819-C-T

9682207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132695-G-A

9682279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132623-T-C

9682334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132570-C-T

9682393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132511-G-A

9682393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132511-G-T

9682647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132325-A-T

9682686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132296-G-A

9682792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132214-T-C

9682813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132189-G-A

9682860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132153-C-T

9682898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132125-C-G

9682898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32132125-C-T

9683129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32131769-T-C

http://identifiers.org/hco/5/GRCh38#9683143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32131755-C-A

9683429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32131357-T-G

9683874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32130938-G-C

9685021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32130717-G-C

9685136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32130595-G-A

9687287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32128288-A-G

9687303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32128270-C-T

9687315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32128258-C-T

9687371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32128182-C-T

http://identifiers.org/hco/5/GRCh38#9688178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32127997-C-A

9692504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118311-A-G

9692655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118174-A-T

9692755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32118078-A-G

9693821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32115156-C-T

9693967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32115011-G-A

9694026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32114935-C-G

http://identifiers.org/hco/5/GRCh38#9694271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32114705-A-C

http://identifiers.org/hco/5/GRCh38#9694437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32114541-A-C

9694794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32113313-T-C

9694890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32113174-A-G

http://identifiers.org/hco/5/GRCh38#9695025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32113069-C-A

9695106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32113004-G-A

9695306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112812-G-T

9695350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112763-T-A

9695430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112677-T-C

9695461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112644-C-T

9695478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112633-T-C

9695494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112595-A-G

9696098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112170-T-C

9696127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112143-A-G

9696142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32112129-A-T

http://identifiers.org/hco/5/GRCh38#9698624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32109993-C-A

9698667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109964-A-G

9698707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109920-G-T

9698708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109919-C-T

9698712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109914-G-A

9698817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109822-G-A

9698817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109822-G-T

9698826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109813-T-G

http://identifiers.org/hco/5/GRCh38#9698888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32109755-A-C

9698910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32109733-T-C

9699227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32108588-T-G

9699321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32108520-G-A

9699588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32108246-T-C

9699646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32108195-T-C

9699877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32107990-A-G

9699887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32107982-C-T

9700015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32107863-A-G

9700107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32107774-C-T

9700202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32107558-A-T

9701257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32105699-C-G

9701340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32105617-C-T

9701502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32105460-T-C

9701656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32105217-G-A

9702171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32104713-G-A

http://identifiers.org/hco/5/GRCh38#9702355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32104527-C-A

9702609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32104316-T-C

9702667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32104262-T-C

9702836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32104125-G-A

9703086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32103900-C-G

9703202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32103782-T-A

9703595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32102721-C-T

http://identifiers.org/hco/5/GRCh38#9703755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32102588-A-C

9703755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32102588-A-T

http://identifiers.org/hco/5/GRCh38#9703898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32102464-C-A

9704052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32102305-T-C

9704097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32102207-T-C

9704188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32102113-A-G

9704200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32102101-C-G

9704418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32101896-A-G

9704439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32101875-C-T

9706869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32099590-G-A

9707026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32099439-G-A

9708077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32098478-A-G

9708085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32098470-G-A

9708085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32098470-G-T

http://identifiers.org/hco/5/GRCh38#9708408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32098146-C-A

9708812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

9708820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

http://identifiers.org/hco/5/GRCh38#9712916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32094978-A-C

http://identifiers.org/hco/5/GRCh38#9712919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32094975-C-A

http://identifiers.org/hco/5/GRCh38#9712922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32094964-C-A

http://identifiers.org/hco/5/GRCh38#9713253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32094643-C-A

9713477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32094418-C-G

9713654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32094233-T-C

9713654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32094233-T-G

http://identifiers.org/hco/5/GRCh38#9713670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32094217-A-C

9713862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32094018-A-G

9714002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32093880-G-A

9714014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32093870-G-T

9714122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32093763-T-C

http://identifiers.org/hco/5/GRCh38#9714152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#32093734-C-A

9714690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32093232-C-G

9714893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32093061-G-T

9715325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092273-A-T

9715527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092110-G-A

http://identifiers.org/hco/5/GRCh38#9716490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32090436-C-A

9716874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32089991-C-T

9717098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32089777-G-C

9717115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32089763-A-G

9717359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32089317-A-G

9722832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085944-C-T

9722869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085907-C-T

9722945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085836-A-G

9722992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085781-G-T

9723000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085766-C-T

9724310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085349-G-A

9724310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085349-G-T

9728715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084782-G-A

9728723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084774-G-A

9728885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084604-G-A

9728885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084604-G-T

9729090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084425-C-T

9729770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083312-C-G

9729894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083234-A-G

9729913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083215-T-C

9729940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083189-T-C

9729996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083136-G-A

9730081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083070-C-G

9730164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082986-T-A

9730164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082986-T-C

http://identifiers.org/hco/5/GRCh38#9730400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32082763-C-A

9730486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082665-C-T

9730505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082643-G-A

9730563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082579-G-A

9730563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082579-G-T

9730567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082575-G-T

9733309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079308-G-A

9733309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079308-G-T

9733413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079212-G-A

9733413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079212-G-T

9733445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079180-A-G

9733482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079136-G-A

9733554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32079067-A-G

9734525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32078465-G-A

9734525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32078465-G-T

http://identifiers.org/hco/5/GRCh38#9737060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32075500-C-A

9737189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32075379-T-C

9737215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32075352-C-T

http://identifiers.org/hco/5/GRCh38#9737355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32073321-C-A

9737412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073263-A-T

http://identifiers.org/hco/5/GRCh38#9737628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32073058-C-A

9737924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072800-T-C

9737929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072795-T-C

9737957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072764-G-A

9738175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072498-G-A

9738253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072420-G-A

9738270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072403-A-G

9738270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072403-A-T

9738271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072402-T-C

9738345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072330-T-G

9738507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072171-C-T

9738585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32072108-T-G

9738812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32071880-G-A

9738867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32071825-A-G

9739448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32071281-G-T

9739724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32070995-C-T

9740193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32070169-T-G

9740488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069898-C-T

9740775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069642-T-C

9741001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069414-T-C

http://identifiers.org/hco/5/GRCh38#9741040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32069375-A-C

9741099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069317-T-C

9741104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069312-C-T

9742183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32068075-C-T

9742273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067977-A-T

9742400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067860-T-C

9742456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32067808-A-G

http://identifiers.org/hco/5/GRCh38#9743611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32066880-A-C

9743795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066693-T-C

9743908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066581-G-T

http://identifiers.org/hco/5/GRCh38#9744415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32066318-A-C

9744553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066184-C-G

9744850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065884-T-C

9744914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065782-T-C

9745058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065641-A-T

http://identifiers.org/hco/5/GRCh38#9745151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32065552-C-A

9745181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065524-A-G

9745204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065501-A-G

9748134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32063670-G-A

http://identifiers.org/hco/5/GRCh38#9748953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32062992-C-A

9748998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062964-A-G

http://identifiers.org/hco/5/GRCh38#9749005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32062955-A-C

9749138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062839-A-G

9749321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062658-G-T

9749544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062464-T-A

9749544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062464-T-C

9749546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062462-G-A

9749546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062462-G-C

9749845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32062204-G-C

9750172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061885-C-T

9750648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32061310-T-C

http://identifiers.org/hco/5/GRCh38#9750881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32061069-A-C

9750967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060972-G-A

9751065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060863-A-T

9751068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060860-T-C

http://identifiers.org/hco/5/GRCh38#9751677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32060257-A-C

9751725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060196-C-G

9751833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060091-A-G

9751875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32060049-C-T

http://identifiers.org/hco/5/GRCh38#9752105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32059808-A-C

9752138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059780-A-G

9752316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059611-G-A

9752371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32059551-C-G

http://identifiers.org/hco/5/GRCh38#9758144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32056477-C-A

9758386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056258-G-A

9758539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056112-C-G

9758553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056098-T-C

9758670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055959-A-G

9759199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055424-G-A

http://identifiers.org/hco/5/GRCh38#9759524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32055125-A-C

9759562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32055087-T-A

9759863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054327-T-A

9760336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32051741-A-G

9760374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32051711-A-G

9760530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32051552-T-C

9760644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32051434-A-G

http://identifiers.org/hco/5/GRCh38#9760709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32051350-A-C

http://identifiers.org/hco/5/GRCh38#9760834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32051249-A-C

9761278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050962-A-G

9761281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050959-T-G

9761386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050912-G-T

9761404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050894-T-A

9761507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050799-C-T

9761622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050667-C-T

9761630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050659-A-G

9761695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050590-C-G

9761695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050590-C-T

9761832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050459-C-G

9761937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050358-T-A

9761971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050318-T-C

9761972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050317-G-C

9762055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32050208-C-T

http://identifiers.org/hco/5/GRCh38#9762312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32049999-A-C

9762488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049828-A-G

http://identifiers.org/hco/5/GRCh38#9762696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32049667-C-A

9762696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049667-C-T

9762792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049578-T-C

9762832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049539-G-C

9762882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049488-T-C

9763178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049206-A-G

9763656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049016-G-A

9763912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048805-A-G

9763964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048753-A-G

9764658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047847-C-T

http://identifiers.org/hco/5/GRCh38#9764755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32047746-C-A

9764755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047746-C-T

http://identifiers.org/hco/5/GRCh38#9764837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32047664-A-C

9765138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047320-G-A

9765345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047119-A-G

9765585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32045946-C-T

9765724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045801-G-T

9766101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045424-C-G

9766101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045424-C-T

9766396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045110-T-G

9766436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045070-G-A

9766449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045060-A-G

9766458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045043-A-T

9766463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045038-A-G

9766587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32044896-C-T

9766767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044713-C-T

9767073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32044376-G-C

9782582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042939-T-C

9782583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042938-T-A

9782722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042793-T-C

9783501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042043-C-T

9783609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32041963-C-T

9784611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040500-G-A

9784672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040441-C-G

9784672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040441-C-T

http://identifiers.org/hco/5/GRCh38#9784744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32040371-C-A

9784883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040223-C-T

9784900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040206-T-C

9784940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040183-A-G

9785072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040078-T-A

9785072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040078-T-C

9785112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040037-G-A

9785501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039678-T-C

http://identifiers.org/hco/5/GRCh38#9785563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32039604-A-C

9785575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039592-T-G

9785641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039520-T-G

9785815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039342-C-G

9785821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039339-C-G

9785859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039301-C-T

9786490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32036566-C-G

9786703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32036379-T-C

9786729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32036354-A-G

9786983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32036098-T-C

9787108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035961-C-G

9787108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035961-C-T

9787261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035825-C-T

9787309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035779-G-A

9787309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035779-G-T

9787536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035554-C-G

9787555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035534-G-A

9787787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035301-C-T

9788152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034954-C-T

9788402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034729-T-C

9788487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034655-T-C

9788599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034557-A-G

9788628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034528-A-G

9788652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034441-G-A

9789035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034084-C-T

9789333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033819-A-G

9789409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033744-A-G

9789483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033670-C-T

9789579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033584-A-G

9789588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033575-T-C

9789690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033486-A-G

9792632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031516-T-C

9792815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031350-C-T

9792840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031331-C-T

9792860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031315-T-C

9792914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031260-T-C

9793004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031181-A-G

9793082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32031106-T-A

http://identifiers.org/hco/5/GRCh38#9793121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32031076-C-A

9793266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030932-T-C

9793277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030921-T-C

9793464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030736-G-A

9793464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030736-G-C

9793752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030511-T-G

9793795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030468-G-T

9793958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030316-A-G

9794241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32030097-A-G

9794356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32029959-G-A

9794356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32029959-G-T

9794517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32029443-A-G

9794732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32029233-C-T

9794854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32029111-T-C

9797460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028895-G-C

9798709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028596-C-T

9798912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028421-C-G

9799099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028354-A-G

9799284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028233-T-A

9799284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028233-T-C

9799286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028231-G-A

9799435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32028045-T-G

9799494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027991-T-A

9799494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027991-T-C

9799634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027865-A-G

9799649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027850-G-A

9799979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027519-T-C

9799992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027506-T-C

9799992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027506-T-G

9800097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027417-C-G

9800117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027367-G-A

9800236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027239-C-T

9800265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027207-T-C

9800421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32027043-G-A

9800575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32025354-G-C

9810659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32024483-G-A

9810826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32024222-C-T

9811037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32024016-C-T

9811117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32023935-C-T

9811155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32023897-C-T

9813597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32023073-T-C

9813756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32022917-T-A

9814411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32021912-T-A

9814492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32021832-T-C

9814583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32021742-T-C

9814801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32021516-T-C

9814994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32021325-A-T

9815280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32021047-G-A

9815360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020991-G-A

9815478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020817-A-G

9815676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020626-C-T

9815768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020517-T-C

9815834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020430-T-C

9815841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020423-A-G

9815925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020354-A-G

9815978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020305-T-C

9816080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020214-C-T

http://identifiers.org/hco/5/GRCh38#9816175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32020137-C-A

9816175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020137-C-G

9816198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32020114-T-C

9816370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32019984-A-T

9816482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32019862-T-G

9816500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32019843-T-G

9816542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32019801-C-T

9816775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32019576-C-G

9816801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32019550-T-C

http://identifiers.org/hco/5/GRCh38#9816941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32019421-A-C

9818150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32017322-G-T

9818255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32017215-G-C

9818256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32017214-T-C

9818577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016910-G-A

9818651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016837-G-C

9818682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016813-C-G

9818794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016723-T-C

http://identifiers.org/hco/5/GRCh38#9818966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32016607-A-C

9819010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016569-G-C

9819028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016549-T-A

9819028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016549-T-G

http://identifiers.org/hco/5/GRCh38#9819029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32016548-C-A

http://identifiers.org/hco/5/GRCh38#9819143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32016483-A-C

9819146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016480-G-A

9819295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016329-T-C

9819357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016278-T-C

9819455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016181-T-C

9819509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32016130-G-A

9820171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32015490-G-T

9820507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32015161-A-G

9820844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32014858-G-T

9821338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32014429-C-T

9821408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32014360-G-A

9821566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32014209-G-A

9821840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32013383-C-T

9822038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32013170-T-A

9822040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32013168-T-G

http://identifiers.org/hco/5/GRCh38#9822048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32013160-A-C

9822191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32013043-A-G

9822199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32013035-C-T

9822370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012944-G-A

9822370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012944-G-T

9822777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012792-T-A

http://identifiers.org/hco/5/GRCh38#9822987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32012576-C-A

http://identifiers.org/hco/5/GRCh38#9822991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32012572-C-A

9822991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012572-C-T

http://identifiers.org/hco/5/GRCh38#9823011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32012559-C-A

9823011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012559-C-T

http://identifiers.org/hco/5/GRCh38#9823072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32012514-C-A

9823125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012460-G-C

9823125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012460-G-T

http://identifiers.org/hco/5/GRCh38#9823183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32012382-A-C

9823347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32012225-C-T

9828635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32009406-T-C

9828924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008909-G-T

9829071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008773-T-C

9829079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008766-C-T

9829365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008480-G-C

9829691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008191-G-A

9829829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008077-T-G

9830058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32008008-G-A

9830074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007993-T-C

9830078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007989-A-G

9830370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007806-A-G

9830407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007775-T-C

9830556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007676-G-A

9830556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007676-G-T

9830567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007663-T-C

9830567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007663-T-G

9830636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007621-T-A

9830636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007621-T-C

http://identifiers.org/hco/5/GRCh38#9830652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32007610-C-A

9830652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007610-C-G

9830724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007544-T-A

http://identifiers.org/hco/5/GRCh38#9830804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32007510-A-C

9830896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007424-G-A

http://identifiers.org/hco/5/GRCh38#9830922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32007398-A-C

9830932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007388-T-C

9830954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007366-T-C

9831021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007293-G-T

9831217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007107-C-T

9831302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32007037-A-T

9831469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006894-A-G

9831613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006759-A-T

http://identifiers.org/hco/5/GRCh38#9831892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#32006552-C-A

9831892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006552-C-T

9832074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006375-A-T

9832090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006357-C-T

9832186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006259-T-C

9832186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006259-T-G

9832261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006178-G-A

9832281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006162-T-C

9832312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006131-G-A

9832385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32006057-T-C

9832497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32005965-C-T

9832672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32005792-T-C

9833651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32005089-T-A

9833651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32005089-T-C

9833740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32004997-A-G

9834373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32004453-T-C

9834829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32004013-G-A

9835168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32003689-G-T

9835239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32003599-T-C

9835712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32003097-A-T

9835845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32002986-T-C

9838146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32001088-A-G

9838338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32000904-G-A

9838926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32000008-T-C

9839001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999956-C-T

9839075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999884-T-C

9839336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999657-T-C

9839447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999538-T-C

9839729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999250-T-A

9839729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999250-T-C

9839788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31999192-C-T

9845661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31996924-G-A

9845662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31996923-G-A

9845825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31996760-G-A

9846140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31996437-G-T

9846206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31996380-A-T

9846492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31995439-G-C

9846521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31995419-C-T

9846888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31994902-C-T

9846914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31994874-C-T

9847244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31994147-A-T

9847479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31993911-A-T

9847554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31993839-T-G

9847849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31993607-G-A

9847991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31993474-G-A

9848024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31993443-A-G

9848493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31992877-C-T

9848580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31992791-A-G

9848625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31992699-T-C

9848881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31992368-C-T

http://identifiers.org/hco/5/GRCh38#9849182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31992121-C-A

9849233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31992077-C-T

9849526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31991453-C-G

http://identifiers.org/hco/5/GRCh38#9849589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31991402-C-A

9849593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31991398-C-T

9849930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31991120-G-A

9849930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31991120-G-C

9849946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31991104-A-G

9850158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31990939-A-T

9852055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31988484-T-A

9852077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31988462-T-C

9852368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31988144-T-G

http://identifiers.org/hco/5/GRCh38#9852476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31988034-C-A

9852628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31987882-T-C

9852777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31987735-G-A

9853032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31987487-G-C

9853059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31987461-G-C

9853789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31987239-G-A

9853903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31987127-T-C

9854326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31986175-T-C

9854425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31986078-T-C

9854475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31986028-T-C

9856145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31985248-G-A

9856238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31985153-A-G

9856292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31985099-A-G

9857944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31981378-G-T

9857990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31981337-G-A

http://identifiers.org/hco/5/GRCh38#9858008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31981319-A-C

9858121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31981221-G-A

9858192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31981097-G-A

9858192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31981097-G-C

9858254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31981053-T-C

9858788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31980599-C-G

9859225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31980163-C-T

9859424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979977-G-A

9859425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979976-T-G

9859509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979913-G-T

9859674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979765-C-T

9859791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31979650-C-G

9859890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979552-T-G

9860225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31978790-G-A

9860624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31978391-G-A

9860919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977791-C-T

9861000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977719-T-C

9861088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977620-A-T

9861099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977609-A-T

9861104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977604-C-T

9861143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977566-C-T

9861425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977311-T-C

9861552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31977190-G-C

9861889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976903-A-G

9861988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976804-T-C

9862018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976774-G-A

9862018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976774-G-C

9862088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31976704-G-A

9862185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976596-A-G

9862369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976419-T-C

9862374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976410-T-A

9862374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976410-T-C

9862377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976407-G-A

9863224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975552-G-T

9863237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975539-T-C

9863261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975515-A-G

9863263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975513-G-A

9863598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975489-G-A

9863605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975482-T-C

9863712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975373-G-T

http://identifiers.org/hco/5/GRCh38#9863826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31975272-C-A

9863826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975272-C-T

9865029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974651-C-T

9865227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974470-A-G

9865238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974459-G-C

9865245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974454-A-G

9865261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974444-T-A

9865324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974396-C-T

9865436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974293-A-G

9865752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973994-T-C

9865906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973840-T-C

9865988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973787-T-C

9866066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973707-C-T

9866146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973664-A-G

9866438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973351-C-T

9866546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973241-G-A

9866546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973241-G-C

9866547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973240-T-C

9866608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973179-T-C

9866612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973175-C-G

9866657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973133-T-G

9866708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973089-C-T

9866715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973081-T-C

9866933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972885-T-C

http://identifiers.org/hco/5/GRCh38#9867092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31972694-C-A

9867092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972694-C-T

9867136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31972650-T-C

http://identifiers.org/hco/5/GRCh38#9867138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31972648-C-A

9867248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972546-G-A

9867248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972546-G-T

9867256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972538-G-A

9867256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972538-G-T

http://identifiers.org/hco/5/GRCh38#9869703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31972417-C-A

9869747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972375-T-A

9870181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31971968-T-C

9870190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31971961-G-A

9870190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31971961-G-T

http://identifiers.org/hco/5/GRCh38#9870203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31971951-C-A

9870203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31971951-C-T

http://identifiers.org/hco/5/GRCh38#9870207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31971947-C-A

9870289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31971878-G-A

9870289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31971878-G-T

9870667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31971511-T-C

http://identifiers.org/hco/5/GRCh38#9870841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31971338-C-A

9870841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31971338-C-T

9871306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31970985-T-C

http://identifiers.org/hco/5/GRCh38#9871830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31970517-A-C

http://identifiers.org/hco/5/GRCh38#9871831-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31970516-A-C

9872377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31969946-A-T

9872459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31969866-T-A

9873041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31969323-C-T

9873331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31969063-T-C

http://identifiers.org/hco/5/GRCh38#9873455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31968857-A-C

9874094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31968704-T-A

9874712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31966198-A-T

http://identifiers.org/hco/5/GRCh38#9874766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31966145-A-C

9874906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31966004-C-T

9874949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31965962-A-T

9875764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31965066-C-T

9875768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31965062-T-A

9875768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31965062-T-G

9876495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31964374-A-T

http://identifiers.org/hco/5/GRCh38#9876538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31964330-C-A

9876563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31964306-T-C

9876602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31964264-T-C

9876894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31963992-G-A

9877262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31962648-A-T

9877936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31962043-T-G

9878122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31961849-A-G

9879081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31961307-T-C

9880136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31958869-C-T

9883453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957678-A-G

9883453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957678-A-T

http://identifiers.org/hco/5/GRCh38#9884584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31957315-C-A

http://identifiers.org/hco/5/GRCh38#9884608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31957291-A-C

9884618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957281-T-A

9884686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957218-C-T

9884690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957214-T-C

9884872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957040-T-C

9884897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31957011-G-A

http://identifiers.org/hco/5/GRCh38#9884950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31956957-A-C

http://identifiers.org/hco/5/GRCh38#9885083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31956830-A-C

9885139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31956625-T-C

http://identifiers.org/hco/5/GRCh38#9885151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31956614-C-A

9885151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31956614-C-T

9885493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31956272-A-T

9885593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31956178-G-C

9885686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31956082-T-G

9887001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31953333-T-C

9887278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31953070-C-T

9887497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31952965-C-T

9887880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31952585-C-T

9887927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31952538-G-A

9888519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31951983-C-T

9888992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31951871-G-A

9889366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31950250-G-T

9889475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31950147-T-C

9889504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31950118-A-G

9889579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31950040-G-A

9889579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31950040-G-T

9889599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31950019-T-C

9889918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31949487-G-T

9890503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31948929-T-C

9890608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 31948835-G-A

9890946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31948499-C-G

9892880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31947436-T-C

http://identifiers.org/hco/5/GRCh38#9892885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31947431-C-A

9892894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31947422-T-C

9892937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31947393-G-T

9893907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31927379-T-C

9895326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31926249-T-C

9895422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31926158-T-C

9895590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31926057-T-C

9895760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31925900-C-T

9897752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922660-T-C

9898000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922410-T-G

9898008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922402-C-G

9898008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31922402-C-T

9898405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31922004-G-A

http://identifiers.org/hco/5/GRCh38#9899009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#31921425-A-C

9899115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31921320-C-T

9900540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31920841-G-A

9901105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31920550-T-A

9901105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31920550-T-C

9901278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31920368-T-C

9901300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31920346-A-G

9901421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31920223-G-A

9901816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31919837-A-T

9901817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31919836-T-C