210022215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759254-C-T

210022333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759365-T-C

210022763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759737-G-T

210022797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759771-A-T

210022805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759779-T-G

210022811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759782-T-C

210022843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759811-A-G

210022858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759825-T-C

http://identifiers.org/hco/2/GRCh38#210022865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66759832-C-A

210022880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759862-G-A

210022880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759862-G-T

http://identifiers.org/hco/2/GRCh38#210022894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66759876-C-A

210022894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759876-C-T

210022899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759885-T-C

210022899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759885-T-G

210022912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3 prime UTR variant
orthologous variants: 66759898-T-G

210023087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: synonymous variant
orthologous variants: 66760073-C-T

http://identifiers.org/hco/2/GRCh38#210023173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66760159-A-C

210023173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 66760159-A-G

http://identifiers.org/hco/2/GRCh38#210023192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66760178-A-C

210023192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66760178-A-G

210023398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66760349-A-G

210023988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66760921-T-C

210024098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 66761029-G-C

210024117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 66761048-A-G

210024142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 66761073-A-T

210024884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762204-A-G

210024999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762317-A-T

210025010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762327-T-C

210025010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762327-T-G

210025054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762371-G-A

210025054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762371-G-C

210025054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762371-G-T

210025225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762547-A-G

210025880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762626-C-T

210025971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762842-G-T

210025986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66762857-A-T

210026163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763016-A-G

210026545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763457-C-G

210027148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763573-T-C

http://identifiers.org/hco/2/GRCh38#210027166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66763591-C-A

210027184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763599-A-G

http://identifiers.org/hco/2/GRCh38#210027225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66763646-C-A

210027225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763646-C-G

210027225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763646-C-T

210027388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763809-T-C

210027388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763809-T-G

http://identifiers.org/hco/2/GRCh38#210027395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66763812-A-C

210027395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66763812-A-G

210027892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66764252-G-C

210027922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66764290-T-C

http://identifiers.org/hco/2/GRCh38#210028499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66764752-C-A

210028499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66764752-C-T

210028543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66764796-G-T

210028690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66764895-A-G

210028724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66764929-C-G

http://identifiers.org/hco/2/GRCh38#210028807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66765002-A-C

210028807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66765002-A-G

210028841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66765029-A-G

210028902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 66765090-G-T

210028937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66765125-G-A

210028937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66765125-G-T

210028963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66765151-C-T

210029051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66765239-T-C

210029051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66765239-T-G

210029111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66765304-T-C

210029160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765347-C-T

http://identifiers.org/hco/2/GRCh38#210029689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66765726-C-A

210029689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765726-C-T

210029750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765787-A-G

210029755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 66765792-T-C

210029973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66766021-G-T

http://identifiers.org/hco/2/GRCh38#210030211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66766259-A-C

210030295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66766313-A-G

210030575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66766607-C-T

210030613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66766660-A-G

210030993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66767224-T-C

210031165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66767360-G-A

210031315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66767494-T-C

210031587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66767785-A-G

210031836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66768061-T-C

http://identifiers.org/hco/2/GRCh38#210031993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66768268-A-C

210032015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66768291-G-T

210032096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66768368-T-C

http://identifiers.org/hco/2/GRCh38#210032373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66768647-C-A

210032441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66768711-G-T

210032460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66768724-A-G

210037191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771007-A-G

210037243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771064-A-G

210037246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771067-A-G

http://identifiers.org/hco/2/GRCh38#210037394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66771196-C-A

http://identifiers.org/hco/2/GRCh38#210037735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66771481-A-C

210037735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771481-A-G

210037743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771490-G-A

210037943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771696-G-A

210038225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66771957-G-A

210039395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66773712-G-A

210039652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66774055-T-C

210039673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66774076-G-C

210040210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66774544-G-T

210040542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66774918-T-A

210040849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66775175-G-T

210041090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66775329-T-C

210041442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66775903-G-A

210041882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66776257-G-A

210041966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66776302-C-T

210041984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66776320-T-C

210042084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66776397-A-G

210042087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66776400-C-T

210042609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66776937-G-T

210044051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66777322-C-T

210051432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66782737-A-G

210051677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66782964-G-A

210051962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66783215-T-G

210052801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66783515-A-T

http://identifiers.org/hco/2/GRCh38#210059312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66785131-C-A

210059493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66785345-T-G

210059802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66785684-C-T

210059903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66785805-G-A

210059972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66785960-A-G

210060023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786015-G-A

210060023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786015-G-T

210060225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786258-A-T

210060232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786265-T-C

210060233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786266-A-G

210060251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786321-A-G

210060273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786343-A-G

210060283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786353-A-G

210060291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786358-T-A

210060322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786388-G-A

http://identifiers.org/hco/2/GRCh38#210060646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66786646-C-A

210060895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66786971-T-C

210060936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66787003-A-G

210061016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66787082-A-G

http://identifiers.org/hco/2/GRCh38#210061056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66787135-C-A

210061416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66787920-C-T

210075505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66801162-C-T

210075627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66801282-G-A

210075627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 66801282-G-T

210076066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66801690-C-T

210076106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66801729-A-G

210076619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66801891-G-C

210076964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66803207-G-A

210085716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66807904-T-C

210085864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66808015-T-C

210085917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66808108-T-C

210086135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66808318-T-C

210086325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66808487-A-G

210086401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66808560-G-A

210086976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66809042-T-A

210086976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66809042-T-G

210097262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811546-A-G

http://identifiers.org/hco/2/GRCh38#210097764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66811715-C-A

210097764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66811715-C-T

http://identifiers.org/hco/2/GRCh38#210097812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66811761-C-A

210097826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66811775-G-A

210097898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811891-T-C

210097913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811907-T-C

210097913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811907-T-G

210097969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811961-G-A

210097969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811961-G-C

210097969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811961-G-T

210097971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66811963-A-G

http://identifiers.org/hco/2/GRCh38#210104074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66812559-A-C

210104161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66812638-T-G

210127837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66815766-G-A

210127837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66815766-G-T

210128123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66816038-G-A

210128603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66816581-G-A

210128888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817007-T-A

210128888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817007-T-C

210128902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817021-T-C

210129073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: synonymous variant
orthologous variants: 66817168-G-A

http://identifiers.org/hco/2/GRCh38#210129144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66817239-C-A

210129144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense variant
orthologous variants: 66817239-C-T

210129308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817396-G-T

210129396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817480-C-T

210129407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817491-T-G

210129697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66817768-A-G

http://identifiers.org/hco/2/GRCh38#210131101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66819434-A-C

210131463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66819762-A-G

210132503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66820925-T-G

210133953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66825945-T-C

210134002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66825991-G-A

210134438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66826329-T-C

210134536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66826410-G-C

210134889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66826707-G-A

210134892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66826710-G-A

210135218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66827325-A-G

210135320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66827427-G-A

210135320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66827427-G-C

210135535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66827753-T-C

210135570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66827788-T-A

210135755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66827941-A-G

210136406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66828502-A-G

210136435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66828531-T-A

210136787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66828852-A-G

210136834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66828941-C-T

210137326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66829376-G-A

210137524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66829540-T-C

210138695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66830224-A-G

210138747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66830274-A-G

210139582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66830809-T-G

210140358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66831246-A-G

210140480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66831362-T-C

210140515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66831392-T-C

210140585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66831454-A-T

210142389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66832663-A-G

210143010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66833465-G-C

210143031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66833486-A-G

210151789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66836416-A-T

210151819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66836446-G-A

210151984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66836610-T-G

210153424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66840138-A-G

210153429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66840143-T-C

210153429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66840143-T-G

210153548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 66840261-A-G

210153931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66840644-C-T

210154219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66840932-T-C

210154219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66840932-T-G

210154315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66841028-T-C

210154315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66841028-T-G

210154495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66841211-T-C

210154841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66841660-A-G

210156340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66842504-C-T

210156610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66842756-A-G

210156841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66842967-A-G

http://identifiers.org/hco/2/GRCh38#210156941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66843075-A-C

210156949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66843086-T-A

http://identifiers.org/hco/2/GRCh38#210156972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66843110-C-A

210157372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66843648-G-A

210158183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66843906-T-C

210158245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66843971-C-T

210158375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66844070-T-G

210158382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66844077-C-G

http://identifiers.org/hco/2/GRCh38#210158565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66844256-C-A

210158565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66844256-C-T

210163732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66849952-C-T

210164543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66850697-C-T

210165217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66851021-A-G

210165226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66851030-G-A

210165468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66851214-G-T

210166408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66851657-T-C

210166618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66851876-A-G

210166809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852025-G-C

210166958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852168-G-A

210166978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852218-G-A

210166978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852218-G-T

210166984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852224-G-A

210167424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852904-C-T

210167461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66852941-G-T

210167564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66853056-A-G

210168003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66853601-A-G

210168003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66853601-A-T

210168517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66854098-A-G

210168588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66854168-A-T

210168920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66854480-C-T

210169192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66854705-A-G

http://identifiers.org/hco/2/GRCh38#210169290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66854786-A-C

210169415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

210169448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66854936-T-C

210169976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66855289-T-G

210170087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66855427-T-C

http://identifiers.org/hco/2/GRCh38#210170146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66855488-C-A

210170252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66855590-T-A

210170287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66855629-A-T

210170312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66855653-G-A

210170312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66855653-G-T

210170433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855795-G-A

210170433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855795-G-T

210170515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855870-G-C

210170515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855870-G-T

http://identifiers.org/hco/2/GRCh38#210170550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66855905-C-A

210170554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855910-G-A

210170572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855928-G-A

http://identifiers.org/hco/2/GRCh38#210170576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66855932-C-A

210170576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855932-C-T

210170614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855970-C-G

210170614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855970-C-T

http://identifiers.org/hco/2/GRCh38#210170628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66855984-C-A

210170632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855988-T-A

210170632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 66855988-T-C

210170672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856026-G-A

210170672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856026-G-C

210170672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856026-G-T

210170681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856035-T-C

210170698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856050-C-T

210170722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856071-C-T

http://identifiers.org/hco/2/GRCh38#210170732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66856077-A-C

210170750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66856101-T-G

http://identifiers.org/hco/2/GRCh38#210170755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66856125-C-A

210170755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66856125-C-T

210170774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66856144-T-C

210170812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66856184-A-G

210170812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: intron variant
orthologous variants: 66856184-A-T

210171230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856614-C-G

210171379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856733-G-A

210171379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 66856733-G-T

210171586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 66856928-G-C

http://identifiers.org/hco/2/GRCh38#210172252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#66857443-A-C

210172631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26310
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66857795-T-C