http://identifiers.org/hco/9/GRCh38#26947049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#94491266-C-A

26947049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94491266-C-G

26947049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94491266-C-T

26947339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 94491552-T-G

http://identifiers.org/hco/9/GRCh38#26947517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#94491730-C-A

26947517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94491730-C-T

26947521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94491734-G-A

26947521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94491734-G-T

http://identifiers.org/hco/9/GRCh38#26947610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#94491822-A-C

26947613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94491834-G-C

26947742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94491962-C-G

26947772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94491981-T-G

26948100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94492356-C-T

26948793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94492690-T-A

26948793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94492690-T-C

26948983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94493122-T-C

26951535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94495237-A-G

26952060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94496778-G-C

26952080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94496798-T-C

26952107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94496813-T-C

26952129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94496835-G-A

26952198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron variant
orthologous variants: 94496899-A-G

26956313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94502645-T-C

26956344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: intron_variant, undefined
orthologous variants: 94502686-T-C

http://identifiers.org/hco/9/GRCh38#26956404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#94502743-C-A

26956404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502743-C-G

26956404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502743-C-T

26956406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502745-C-T

26956409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502748-G-C

26956409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502748-G-T

26956414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502753-T-C

26956512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502884-C-G

26956512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502884-C-T

26956541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94502906-T-C

26956582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502947-G-A

26956582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502947-G-T

26956585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502950-G-A

26956585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502950-G-T

http://identifiers.org/hco/9/GRCh38#26956589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94502954-C-A

26956589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502954-C-T

26956590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502955-G-A

26956590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94502955-G-T

26956640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 94503010-G-T

26956718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503043-C-G

26956771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503091-C-T

26956779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503099-T-C

26956860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503152-C-T

26956978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503272-G-T

26957103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503400-A-G

26957293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503532-G-A

26957293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503532-G-T

26957539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503732-T-C

26957658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503869-A-G

26957675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503877-T-C

26957730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94503911-G-A

26957826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504050-C-T

26958254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504595-G-A

26958279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504620-G-C

26958296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504637-A-G

26958371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504697-C-T

26958419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504745-A-G

26958498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94504828-G-A

26958916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94505153-C-T

26959409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94505384-G-A

26959496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94505455-A-G

26959595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94505549-G-T

26959655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94505632-G-A

26959803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94505781-T-C

26961828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506066-G-A

26961828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506066-G-C

26961828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506066-G-T

26961842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506081-A-G

26961860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506104-T-A

26962010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 94506261-A-G

26962057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94506308-C-G

26962057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94506308-C-T

26962060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94506311-A-G

26962207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506409-T-A

26962207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506409-T-C

26962226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506428-T-C

26962227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506429-G-T

26962242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506435-A-G

26962252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506445-G-A

26962252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506445-G-T

http://identifiers.org/hco/9/GRCh38#26962426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94506553-A-C

26962563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506686-A-G

26962862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506962-A-G

http://identifiers.org/hco/9/GRCh38#26962880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94506980-C-A

26962880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94506980-C-T

26970237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94508514-T-G

26970342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94508619-T-G

http://identifiers.org/hco/9/GRCh38#26970546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94508791-A-C

26978036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94509999-T-A

26978036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94509999-T-C

26978193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94510156-T-C

26978306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94510256-G-A

26978306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94510256-G-T

26978408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94510352-G-A

26979145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94511831-A-G

26979210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94511864-A-G

26980370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94512783-G-A

26980370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94512783-G-C

26980370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94512783-G-T

26980399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94512811-G-A

26980516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94512918-G-T

26982143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94514241-A-T

http://identifiers.org/hco/9/GRCh38#26982223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94514319-C-A

26982223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94514319-C-T

26982293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94514388-T-C

26982293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94514388-T-G

26982298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 94514394-T-C

26982382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 94514461-G-A

26982382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94514461-G-T

26982436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94514501-T-A

26982436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94514501-T-C

26983809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94514859-T-A

26983809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94514859-T-G

26983879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94514924-A-G

26983929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94514970-G-A

26983929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94514970-G-T

26983968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94515012-G-A

26983968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94515012-G-C

26983968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94515012-G-T

26984102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94515079-A-G

26984102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94515079-A-T

26984135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94515108-T-C

26984332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94515289-A-G

26984398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94515401-A-G

26984573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94515565-T-A

26985852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516315-A-G

26985870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516333-T-C

26986194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516554-T-C

26986424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516749-T-A

26986918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516800-C-G

26986919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516801-A-G

26987015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94516891-G-A

26988256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94520547-A-G

26988388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94520667-G-A

26988563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94520814-G-A

26988563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94520814-G-T

26988639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94520882-G-A

26988780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94521026-A-G

26989181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94522670-T-A

26990151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94524028-T-C

26990184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94524061-T-A

26990184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 94524061-T-C

26990394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94524635-A-G

26990454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94524692-T-C

26993757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94524956-T-A

26993757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94524956-T-C

26993757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94524956-T-G

http://identifiers.org/hco/9/GRCh38#26993784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94524983-C-A

http://identifiers.org/hco/9/GRCh38#26994033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94525214-C-A

http://identifiers.org/hco/9/GRCh38#26994684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94525656-A-C

26994775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525743-G-A

26994775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525743-G-T

26994807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525774-T-C

26994807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525774-T-G

26994869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525838-T-C

26994878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525849-G-C

26994900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525861-G-A

http://identifiers.org/hco/9/GRCh38#26994914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94525875-C-A

26994914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525875-C-G

26994930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94525896-C-G

http://identifiers.org/hco/9/GRCh38#26995132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94526070-C-A

26995354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94526301-C-G

26995354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94526301-C-T

26995400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94526344-T-A

26995482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94526425-G-A

26995482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94526425-G-T

26995506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94526448-A-T

26995594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 94526534-G-C

26995753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94526693-G-C

26995753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94526693-G-T

http://identifiers.org/hco/9/GRCh38#26995756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94526696-C-A

26995756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94526696-C-T

26996240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94527373-T-C

26996294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94527427-T-A

26996294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94527427-T-C

26996361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94527494-A-G

26996365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 94527498-G-A

26996383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94527504-G-T

26996435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 94527556-T-C

26996452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94527573-A-G

26996490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 94527611-T-G

26996665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94527989-T-G

26997744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94528708-T-C

26997752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94528716-A-G

26998029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 94528993-A-G

26998066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94529030-G-C

26998208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94529172-T-C

26998208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94529172-T-G

26998235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 94529199-G-A

26998235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 94529199-G-T

26998250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94529214-A-G

http://identifiers.org/hco/9/GRCh38#26998302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94529254-A-C

26998302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94529254-A-G

26998495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94529412-T-C

26999714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94531630-A-G

26999717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94531633-G-A

26999717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94531633-G-T

27003847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94536523-A-T

27004265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94537012-A-G

27004370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94537091-A-G

27004941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94537507-G-A

http://identifiers.org/hco/9/GRCh38#27005225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94537784-A-C

27005225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94537784-A-G

http://identifiers.org/hco/9/GRCh38#27005339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94538083-A-C

27005339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94538083-A-G

27005339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94538083-A-T

27005450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94538161-G-A

27005477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94538188-T-A

27007144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94539122-T-C

27007179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94539162-C-T

27007314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94539293-A-G

27007314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94539293-A-T

http://identifiers.org/hco/9/GRCh38#27008240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94540528-C-A

27008754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94540980-T-A

27008800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541023-A-G

27008829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541049-T-C

27008916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541082-A-G

27009179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541323-G-A

27009179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541323-G-C

27009304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541439-A-G

27009781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94541844-G-A

http://identifiers.org/hco/9/GRCh38#27011518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94542798-A-C

27011856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543034-T-C

http://identifiers.org/hco/9/GRCh38#27011898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94543058-C-A

27011898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 94543058-C-T

27011929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 94543089-A-G

27011929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 94543089-A-T

27011932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 94543092-G-T

27011979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543139-A-G

27012002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543159-A-G

27012002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543159-A-T

27012006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543163-A-G

27012007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543164-G-A

27012007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94543164-G-T

27016884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94546726-T-C

http://identifiers.org/hco/9/GRCh38#27016975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94546812-C-A

27016975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 94546812-C-T

27017268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94547005-G-C

http://identifiers.org/hco/9/GRCh38#27017304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94547010-C-A

27017686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94547401-A-G

http://identifiers.org/hco/9/GRCh38#27017808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94547509-C-A

27018480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549110-G-A

27018576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549113-G-T

http://identifiers.org/hco/9/GRCh38#27018593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94549130-A-C

27018593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549130-A-G

http://identifiers.org/hco/9/GRCh38#27018596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94549133-C-A

27018596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549133-C-G

27018596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549133-C-T

27018599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549138-A-G

27018643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 94549181-G-A

27018643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 94549181-G-T

27018786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549331-A-G

27018834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549401-A-G

27018959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94549527-T-G

27029143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94550943-G-A

27029162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94550968-G-A

27029162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94550968-G-C

http://identifiers.org/hco/9/GRCh38#27029238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94551039-C-A

27029325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94551134-C-T

27031593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94555613-A-T

27032213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94555792-T-C

27032438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94556136-A-T

27032497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94556389-T-C

27032589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94556481-C-T

27032781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94556680-G-A

27032798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94556697-A-G

27033035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94556806-C-G

27033310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557542-C-T

27033326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557557-G-A

27033326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557557-G-C

27033326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557557-G-T

27033342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557572-G-A

27033439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557694-T-A

27033536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557763-T-C

http://identifiers.org/hco/9/GRCh38#27033555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94557787-C-A

27033555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94557787-C-G

27033878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94558003-A-G

27033962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94558090-C-T

27033990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94558125-G-T

27034068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94558203-G-A

27034068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94558203-G-T

27035252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561358-A-G

27035409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561494-G-T

27035433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561514-C-T

27035500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561567-A-G

27035565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561629-G-A

27035565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561629-G-T

27035617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561665-C-G

27035760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94561816-T-C

27039886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94562444-C-T

27041825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94564201-C-G

27041825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94564201-C-T

27041905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94564273-G-A

27042520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94564785-T-C

27042689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94564953-C-T

27043858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94565888-A-G

27044271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566051-C-G

27044503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566257-G-C

27044567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566324-C-G

http://identifiers.org/hco/9/GRCh38#27044593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94566345-C-A

27044593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566345-C-G

http://identifiers.org/hco/9/GRCh38#27044625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94566388-C-A

27044625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566388-C-G

27044625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566388-C-T

27044714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566479-T-A

27044714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94566479-T-C

27044783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94566543-G-A

27044783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 94566543-G-T

27046741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94567235-C-G

http://identifiers.org/hco/9/GRCh38#27046779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94567265-A-C

27046779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94567265-A-G

27047244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94567385-G-A

27047845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94567955-C-T

27047853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94567962-A-T

27047934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94568039-A-G

27048085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94568124-G-C

27048106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94568142-A-G

http://identifiers.org/hco/9/GRCh38#27048122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94568147-C-A

27048122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94568147-C-T

27048210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94568233-T-C

http://identifiers.org/hco/9/GRCh38#27048213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94568236-C-A

27048225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94568248-A-G

27048279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94568302-G-A

http://identifiers.org/hco/9/GRCh38#27051573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94570406-A-C

27051573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570406-A-G

27051573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570406-A-T

27051612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570444-G-A

27051612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570444-G-C

27051658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570488-A-G

27051809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570548-T-A

27051951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94570684-C-G

27052775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94571138-T-C

27052880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94571225-T-C

27053349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94571533-G-C

27053990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94572280-C-T

27053991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94572281-G-A

27054060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94572328-A-T

27054129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94572396-C-T

http://identifiers.org/hco/9/GRCh38#27055835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94574563-A-C

27055835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94574563-A-T

http://identifiers.org/hco/9/GRCh38#27055914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94574644-C-A

27055914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94574644-C-G

27056104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94574822-C-G

http://identifiers.org/hco/9/GRCh38#27056150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94574869-A-C

27056189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94574907-G-T

http://identifiers.org/hco/9/GRCh38#27056199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94574917-C-A

27056199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94574917-C-G

27056304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94575025-A-G

http://identifiers.org/hco/9/GRCh38#27056428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94575142-C-A

http://identifiers.org/hco/9/GRCh38#27056569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94575326-C-A

27056612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94575361-A-G

27056670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94575418-A-G

27056753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94575503-A-G

27056753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94575503-A-T

27057135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94577245-G-A

27057199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94577308-G-T

27057206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94577312-T-G

27057265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94577350-C-T

http://identifiers.org/hco/9/GRCh38#27057326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94577412-A-C

27057340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94577426-C-T

27059159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94578615-A-G

27059309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94578764-A-G

27059480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94578917-G-C

27059517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94578938-A-G

27059602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579022-C-G

27059667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579081-A-G

27059688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579098-A-G

27059707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579118-A-G

http://identifiers.org/hco/9/GRCh38#27060155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#94579535-A-C

27060292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579672-G-A

27060292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579672-G-C

27060315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579690-A-G

27060488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579859-A-G

27060534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579900-G-C

27060534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94579900-G-T

27061130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94580086-T-C

27061302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94580250-C-G

27061765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 94580415-G-A

27062134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94580696-G-A

27062176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94580739-G-T

27062350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94580906-C-T

27062405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 94580976-A-T

27062818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94581359-G-A

27062818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94581359-G-C

27062818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94581359-G-T

27062822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94581363-A-G

27062859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94581402-T-A

27062874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 94581417-T-C

27065275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3 prime UTR variant
orthologous variants: 94585193-C-T

27065445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21424
most severe consequence: 3 prime UTR variant
orthologous variants: 94585361-A-G