138501892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 5 prime UTR variant
orthologous variants: 23462024-G-A

138501892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 5 prime UTR variant
orthologous variants: 23462024-G-T

138501982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 23461935-G-C

138502057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 23461879-G-A

138502232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461807-G-A

138502232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461807-G-C

138502232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461807-G-T

138502298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461771-G-A

http://identifiers.org/hco/2/GRCh38#138502354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23461722-A-C

138502389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461689-G-T

138502396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461682-T-G

138502409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461677-C-T

138502417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461669-C-G

138502421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461665-C-G

138502421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461665-C-T

138502443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461645-T-C

138502447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461641-C-T

138502734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461418-C-T

http://identifiers.org/hco/2/GRCh38#138502756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23461387-C-A

138502756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461387-C-T

138502795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461347-T-C

138502795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461347-T-G

138502809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461332-A-G

138502809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461332-A-T

138502839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461308-G-C

138502963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23461197-C-G

138503229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460944-C-G

138503229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460944-C-T

138503290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460891-T-C

138503313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460868-A-G

138503339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23460848-C-T

138503483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460709-A-T

138503508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460684-C-T

138505030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460240-G-T

138505121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23460174-A-G

138505219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23460099-T-C

http://identifiers.org/hco/2/GRCh38#138505266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#23460053-C-A

138505266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23460053-C-T

138505325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23459994-T-A

138509109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23458098-G-A

138509222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23458004-A-G

138510205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23456924-G-T

138510321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23456811-T-G

138514877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23452046-G-A

138514877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23452046-G-C

138515192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23451768-G-T

138515306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23451664-G-C

138515681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23451294-A-G

138516041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23450419-A-G

138516277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23450225-G-A

138516414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23450129-T-C

138516442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23450100-A-G

138516688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449939-A-G

138516773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449881-A-T

138516789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449865-A-G

138516832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449831-G-T

138517022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449663-G-A

138517207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449500-G-C

138518131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23449002-T-G

138518254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23448894-G-A

138520383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23446028-T-C

138520630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23445095-T-C

138520759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23444968-G-A

138545974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23440713-G-A

138546006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23440681-C-T

138546118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23440593-G-A

138546334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23440173-T-G

138546565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23439923-G-C

138546574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23439914-T-C

http://identifiers.org/hco/2/GRCh38#138546629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23439865-C-A

138546629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23439865-C-T

138546715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23439782-C-G

http://identifiers.org/hco/2/GRCh38#138549483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23436114-C-A

http://identifiers.org/hco/2/GRCh38#138550137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23435607-C-A

138550341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23435406-A-G

138550779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23435021-G-T

138550810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434987-G-A

138550810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434987-G-T

http://identifiers.org/hco/2/GRCh38#138550815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23434982-C-A

138550815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434982-C-G

138550815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434982-C-T

http://identifiers.org/hco/2/GRCh38#138550819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23434978-C-A

138550819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434978-C-G

138550819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434978-C-T

138550822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434975-T-G

138550827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434971-T-C

138550827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434971-T-G

138550878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434931-A-G

138550878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434931-A-T

138551184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434650-G-T

http://identifiers.org/hco/2/GRCh38#138551203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23434627-C-A

138551203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434627-C-T

138551355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434477-A-G

138551390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434445-G-C

138551467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434388-T-G

http://identifiers.org/hco/2/GRCh38#138551540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23434323-C-A

138551697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23434175-T-A

138551923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23433994-A-G

138552331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23433538-G-A

138552467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23433415-T-C

138552729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23433158-T-C

138553116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432828-T-A

138553116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432828-T-G

138553267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432668-A-G

138553304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432638-T-G

138553946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432106-A-T

138553982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432065-T-C

138553991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23432056-T-G

138554081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431979-T-A

138554081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431979-T-G

138554089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431971-G-A

138554089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431971-G-T

138554203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431844-C-T

138554241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431805-C-T

http://identifiers.org/hco/2/GRCh38#138554379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23431684-C-A

http://identifiers.org/hco/2/GRCh38#138554397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23431667-C-A

138554428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431636-T-C

138554469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 23431595-A-G

138554610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431462-A-G

138554611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431461-G-A

138554611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431461-G-T

138554737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431342-T-C

138554862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431216-G-C

138555491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431052-A-G

138555498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23431045-A-G

138555668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23430884-G-T

138555826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23430723-A-G

http://identifiers.org/hco/2/GRCh38#138555987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23430649-C-A

138556235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23430490-T-A

138556340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23430368-T-A

138556375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23429915-A-G

138556535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23429761-C-G

138556539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23429757-T-C

138556797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23429509-T-C

138556797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23429509-T-G

138558301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23428563-A-G

http://identifiers.org/hco/2/GRCh38#138558316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23428548-C-A

138558625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23428043-T-A

138558625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23428043-T-C

138558647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23428021-G-C

138558799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427878-T-C

138558894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427775-G-T

http://identifiers.org/hco/2/GRCh38#138559221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23427451-A-C

138559232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427442-T-C

138559368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427303-T-A

138559396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427273-T-C

138559457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427225-T-A

138559457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427225-T-G

138559460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427222-A-G

http://identifiers.org/hco/2/GRCh38#138559463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23427219-C-A

138559463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427219-C-T

138559549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427136-A-G

138559605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427088-G-A

http://identifiers.org/hco/2/GRCh38#138559613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23427080-C-A

138559613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427080-C-G

138559653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23427044-T-C

138560648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23408055-T-G

http://identifiers.org/hco/2/GRCh38#138560702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23408042-A-C

138560702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23408042-A-G

http://identifiers.org/hco/2/GRCh38#138560713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23408031-A-C

138560713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23408031-A-G

http://identifiers.org/hco/2/GRCh38#138560728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23408030-C-A

138560728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23408030-C-G

138560767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23407998-T-A

http://identifiers.org/hco/2/GRCh38#138560955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23407811-A-C

138560959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23407784-T-C

138560964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23407779-T-G

138561037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23407687-G-T

138561063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23407661-G-T

http://identifiers.org/hco/2/GRCh38#138561208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23407542-A-C

138561342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23407431-G-T

http://identifiers.org/hco/2/GRCh38#138564525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23405482-C-A

138564556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23405452-T-A

http://identifiers.org/hco/2/GRCh38#138564579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23405431-C-A

138564579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23405431-C-T

138564650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23405360-T-C

138564856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405152-C-T

138564876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23405132-G-A

138565051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23405008-T-C

138565071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23404988-T-C

http://identifiers.org/hco/2/GRCh38#138565108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#23404958-C-A

138565130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23404936-A-G

138565186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23404890-C-T

138565682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23403587-A-T

138566724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23403171-T-C

138567688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23402513-C-G

138567890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23402379-T-A

138567890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23402379-T-G

138567912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23402361-G-A

138568081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23402215-A-G

138568201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23402105-A-T

http://identifiers.org/hco/2/GRCh38#138568403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23401914-C-A

138568414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23401903-T-C

http://identifiers.org/hco/2/GRCh38#138568435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23401882-C-A

http://identifiers.org/hco/2/GRCh38#138568548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23401797-A-C

138568878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23401525-G-A

138568915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23401491-T-C

138568915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23401491-T-G

138569085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 23401322-T-A

138569085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 23401322-T-C

http://identifiers.org/hco/2/GRCh38#138569094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23401313-C-A

138569094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 23401313-C-G

138569094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 23401313-C-T

138569105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 23401303-T-C

138569143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23401267-T-C

138569171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 23401241-T-G

138569261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23401156-T-A

http://identifiers.org/hco/2/GRCh38#138569367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23401052-C-A

138569617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23400812-C-T

138570061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23400366-G-T

http://identifiers.org/hco/2/GRCh38#138570593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23400237-A-C

138570923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23398474-T-C

138571071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23398345-C-G

http://identifiers.org/hco/2/GRCh38#138571272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23398184-C-A

138571360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23398115-G-C

138571376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23398099-A-G

138571436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23398038-C-T

138571657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23397817-A-G

138571683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23397779-A-G

138571813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23397651-T-C

138571910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23397551-A-T

138572493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396909-G-T

138572494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396908-T-G

138572516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396886-T-G

138572547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396879-T-G

http://identifiers.org/hco/2/GRCh38#138572550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23396876-A-C

138572557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396869-A-G

138572584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396842-C-T

138572614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396813-T-C

138572630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396803-G-A

138572686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396759-A-G

138572693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396752-A-G

138572956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396493-A-G

http://identifiers.org/hco/2/GRCh38#138573275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#23396192-C-A

138573288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396178-G-A

138573350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396132-T-C

138573359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396123-G-A

138573359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396123-G-C

138573359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27934
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23396123-G-T