139495806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415601-A-G

139495817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415612-G-A

139495817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415612-G-T

139495870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415665-G-T

139495920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415719-C-T

139495985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415788-A-G

http://identifiers.org/hco/4/GRCh38#139496049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51415848-C-A

http://identifiers.org/hco/4/GRCh38#139496084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51415881-C-A

139496084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415881-C-G

139496084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3 prime UTR variant
orthologous variants: 51415881-C-T

http://identifiers.org/hco/4/GRCh38#139496092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51415888-C-A

139496092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415888-C-G

139496092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415888-C-T

139496112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415908-T-A

139496112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415908-T-C

139496112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415908-T-G

http://identifiers.org/hco/4/GRCh38#139496158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51415955-C-A

139496158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415955-C-G

139496158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415955-C-T

139496172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415969-G-A

139496172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415969-G-T

139496190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415989-G-A

139496190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415989-G-C

139496190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415989-G-T

139496229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51415999-G-T

139496341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51416075-T-C

139496341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 51416075-T-G

http://identifiers.org/hco/4/GRCh38#139496434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51416168-C-A

139496484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 51416217-T-C

139496605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416334-A-T

139496629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416357-G-C

139496629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416357-G-T

139496695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416425-C-T

139496875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416568-C-T

139496891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416600-T-C

139496904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416613-A-G

139496908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51416617-C-T

139497572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51418075-G-A

139497851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51418382-C-T

139497945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51418471-C-T

139506023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51422718-G-T

139506060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51422761-C-G

http://identifiers.org/hco/4/GRCh38#139506354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51423064-C-A

139506515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51423248-G-A

http://identifiers.org/hco/4/GRCh38#139506676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51423383-C-A

139506949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51423653-A-T

139507383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51424067-T-A

139507732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51424501-A-T

139507932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51424731-A-G

http://identifiers.org/hco/4/GRCh38#139507955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#51424753-C-A

139508058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51424861-G-T

139508192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425073-G-A

139508192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425073-G-T

139508228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425122-T-C

139508342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425243-G-T

139508414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425313-G-T

139508535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425447-A-G

139508720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425639-A-G

139508913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425797-A-G

139508963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425873-A-G

139508982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425891-G-A

139508982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425891-G-T

139508989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425898-T-A

139508989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425898-T-C

139508989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425898-T-G

139508994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425903-A-G

139508997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425906-A-G

139509058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425983-G-A

139509058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425983-G-T

http://identifiers.org/hco/4/GRCh38#139509072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51425997-C-A

139509072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51425997-C-T

139509080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426005-C-T

139509081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426006-A-G

139509162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426145-G-A

139509162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426145-G-T

http://identifiers.org/hco/4/GRCh38#139509275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51426222-C-A

139509275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426222-C-T

139509284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426231-T-C

139509544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426636-A-T

139509552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426644-T-C

139509558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426649-G-A

139509558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426649-G-T

139509566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426657-G-C

139509566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426657-G-T

http://identifiers.org/hco/4/GRCh38#139509578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51426664-C-A

139509578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426664-C-T

http://identifiers.org/hco/4/GRCh38#139509598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51426684-C-A

139509598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426684-C-T

139509815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51426883-T-C

http://identifiers.org/hco/4/GRCh38#139509907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51426973-C-A

139509987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427048-C-T

139510037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51427112-G-A

139510108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427181-G-A

139510124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427197-T-C

139510234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427310-A-G

139510274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427349-G-A

139510274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427349-G-T

139510306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427359-G-A

139510306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427359-G-T

139510349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427390-A-G

139510433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427472-G-T

139510439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427478-A-G

139510451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427490-T-G

139510507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427534-A-T

http://identifiers.org/hco/4/GRCh38#139510939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51427956-C-A

139510939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51427956-C-T

139511021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428036-G-T

139511038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428053-T-C

139511052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428066-A-G

http://identifiers.org/hco/4/GRCh38#139511205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51428222-C-A

139511306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428317-A-G

139511315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428326-T-C

http://identifiers.org/hco/4/GRCh38#139511318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51428329-C-A

139511348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428365-G-T

139511393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428410-G-C

139511393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428410-G-T

139511471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428481-G-A

139511471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 51428481-G-C

139511768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 51428833-G-A

139511783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 51428848-G-A

139511783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 51428848-G-C

139511821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 51428886-G-A

http://identifiers.org/hco/4/GRCh38#139511883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51428948-C-A

139511883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51428948-C-G

139511911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51428970-G-T

http://identifiers.org/hco/4/GRCh38#139511979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51429020-C-A

139511979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51429020-C-T

139511985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51429027-G-A

139511985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51429027-G-T

139513702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51429808-T-A

139513724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51429830-C-T

139514479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51431837-T-A

139514479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51431837-T-C

139514645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51431954-T-C

139515288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51432362-C-T

139515390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51432478-G-A

139515406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51432494-C-G

139515492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51432556-G-A

139515676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51432732-C-T

139515802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51432859-T-G

139517613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434027-G-A

139517764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434140-G-T

139517789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434174-G-A

139517789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434174-G-T

139517829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434213-T-C

http://identifiers.org/hco/4/GRCh38#139517968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51434349-C-A

139518122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434503-T-C

139518566-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434618-T-A

139518566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51434618-T-C

139519940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51437286-A-T

139520266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51437482-G-A

139520266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51437482-G-C

139520266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51437482-G-T

139520325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51437540-A-G

http://identifiers.org/hco/4/GRCh38#139520432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51437655-C-A

139520432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51437655-C-G

139520432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51437655-C-T

139520439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51437662-T-C

139520549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51437756-T-C

139520578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51437785-G-A

139520654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438413-C-G

139520663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438421-T-C

139520712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438468-T-C

139520858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438581-T-G

139520921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438629-T-G

139521015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438720-G-A

139521056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438760-T-C

139521119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51438814-A-G

139521858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51439266-G-A

139522198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51439604-C-T

139522231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51439636-C-T

139522309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51439690-T-G

139522491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51439785-G-A

139523219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440273-G-A

139523219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440273-G-T

http://identifiers.org/hco/4/GRCh38#139523259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51440314-C-A

139523283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440338-A-G

http://identifiers.org/hco/4/GRCh38#139523493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51440567-C-A

139523493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440567-C-T

139523509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440585-T-C

139523512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440588-G-A

139523512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51440588-G-T

139524281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51441410-T-C

139524351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51441481-G-T

139528354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51443287-C-T

139528440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51443392-A-T

139528501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51443431-C-T

139528893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51443785-G-T

139528937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51443827-A-G

http://identifiers.org/hco/4/GRCh38#139529038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51443894-C-A

139529038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: missense variant
orthologous variants: 51443894-C-G

139529125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: synonymous variant
orthologous variants: 51443981-A-G

139529182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 51444038-C-G

http://identifiers.org/hco/4/GRCh38#139529234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51444090-C-A

http://identifiers.org/hco/4/GRCh38#139529241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51444096-C-A

139529318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444179-G-A

139529318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444179-G-T

139529324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444185-G-A

139529324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444185-G-T

139529406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444251-T-C

139529406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444251-T-G

139529495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444343-G-C

139529529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444379-G-T

139529540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51444389-T-C

139530068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51446340-G-C

139530197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51446449-A-G

139530352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51446595-C-T

139530413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51446697-T-A

139530561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51446795-C-T

139530669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51446908-G-A

http://identifiers.org/hco/4/GRCh38#139530692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51446934-C-A

139530826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51447293-T-A

139530830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51447307-T-G

139530832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51447309-G-A

139530832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51447309-G-T

139531031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, undefined
orthologous variants: 51447489-G-A

139531031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, undefined
orthologous variants: 51447489-G-C

139531031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, undefined
orthologous variants: 51447489-G-T

139531698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51448585-G-C

http://identifiers.org/hco/4/GRCh38#139532988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51449882-A-C

139532988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51449882-A-T

139533039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51449931-G-A

139533039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51449931-G-T

139533097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51449967-T-C

139533128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51450011-G-A

139533128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51450011-G-T

139533312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51450200-A-G

http://identifiers.org/hco/4/GRCh38#139533354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51450242-C-A

139533354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 51450242-C-T

http://identifiers.org/hco/4/GRCh38#139533408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51450409-A-C

139533414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450424-C-G

139533414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450424-C-T

139533433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450522-C-T

http://identifiers.org/hco/4/GRCh38#139533473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51450564-C-A

139533473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450564-C-G

139533473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450564-C-T

139533479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450570-T-C

139533779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51450927-G-A

139534034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51451330-G-A

139534101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51451398-G-A

http://identifiers.org/hco/4/GRCh38#139534311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51451593-A-C

139534661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51451872-G-A

139534712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51451923-G-A

139535262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51452571-G-C

139535363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51452674-T-C

139538766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51454218-T-C

139539080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51454563-T-C

139544495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51456512-G-C

139544623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51456624-C-T

139544853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51456818-G-A

139545157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457130-A-G

139545179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457152-G-A

139545181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457154-G-A

139546728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457458-G-T

139546801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457530-A-T

139546869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457598-C-T

http://identifiers.org/hco/4/GRCh38#139547076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51457827-C-A

139547076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457827-C-G

139547076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457827-C-T

139547084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457835-T-C

139547091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457859-T-C

http://identifiers.org/hco/4/GRCh38#139547093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51457867-C-A

139547093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457867-C-T

http://identifiers.org/hco/4/GRCh38#139547098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51457872-C-A

139547098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457872-C-T

139547108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457893-G-A

139547108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457893-G-T

139547123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457920-T-C

http://identifiers.org/hco/4/GRCh38#139547128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51457925-C-A

139547128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51457925-C-T

139547201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51458004-G-A

139547201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51458004-G-C

139547201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51458004-G-T

139547229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51458047-C-T

139547261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51458078-T-C

139547309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51458129-A-G

http://identifiers.org/hco/4/GRCh38#139548019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51458266-C-A

139548797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51459020-A-G

http://identifiers.org/hco/4/GRCh38#139549105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51459254-A-C

139551337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461215-G-A

139551396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461270-G-A

139551396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461270-G-T

139551484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461350-C-T

139551693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461521-T-C

139552282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461804-G-A

139552378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51461909-C-T

http://identifiers.org/hco/4/GRCh38#139552407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51461947-C-A

139552590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51462085-G-C

139552611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51462106-C-T

139552656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51462155-T-C

139552696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51462238-G-A

139552739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51462285-C-T

139552763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51462312-A-G

139553377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51463938-T-C

139553486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51464047-C-T

139554171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51465636-T-G

139554305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51465869-C-G

139554479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51466329-A-T

139555121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51466985-A-G

139555179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467056-T-A

139555202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467079-T-A

139555202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467079-T-G

http://identifiers.org/hco/4/GRCh38#139555215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51467092-C-A

139555516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467344-C-T

139555842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51467680-G-A

139555880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467718-G-A

http://identifiers.org/hco/4/GRCh38#139556016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51467852-C-A

139556016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467852-C-T

139556076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467917-G-A

139556076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51467917-G-T

139556145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51467986-G-A

http://identifiers.org/hco/4/GRCh38#139556183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468023-C-A

139556183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468023-C-G

139556183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468023-C-T

139556339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468190-G-A

139556339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468190-G-T

http://identifiers.org/hco/4/GRCh38#139556349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468200-C-A

139556349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468200-C-G

http://identifiers.org/hco/4/GRCh38#139556350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468201-C-A

139556350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468201-C-T

http://identifiers.org/hco/4/GRCh38#139556353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468204-C-A

139556353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468204-C-T

139556409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468240-G-A

139556409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468240-G-C

139556409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468240-G-T

http://identifiers.org/hco/4/GRCh38#139556493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468324-C-A

139556493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468324-C-T

139556597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468425-G-A

139556597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468425-G-T

http://identifiers.org/hco/4/GRCh38#139556600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468428-C-A

139556600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468428-C-T

139556630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468448-C-T

139556648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468466-C-G

139556709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468548-C-T

139556754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468595-T-C

139556756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468597-G-A

139556756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 51468597-G-T

139556789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51468637-A-G

http://identifiers.org/hco/4/GRCh38#139556822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468666-C-A

139556822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468666-C-T

http://identifiers.org/hco/4/GRCh38#139556824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468668-C-A

139556824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468668-C-T

139556844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468688-C-T

http://identifiers.org/hco/4/GRCh38#139556868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468717-C-A

139556868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468717-C-G

139556895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 51468743-G-T

http://identifiers.org/hco/4/GRCh38#139556909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468757-C-A

139556910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468758-G-A

139556910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468758-G-T

139556977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468836-G-C

139556977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468836-G-T

http://identifiers.org/hco/4/GRCh38#139556980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468839-C-A

139556980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468839-C-T

139556982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468841-G-T

http://identifiers.org/hco/4/GRCh38#139557067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468928-C-A

http://identifiers.org/hco/4/GRCh38#139557114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468964-C-A

http://identifiers.org/hco/4/GRCh38#139557130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51468980-C-A

139557130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51468980-C-T

139557188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469028-G-A

139557188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469028-G-T

139557216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469056-T-C

139557261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469101-C-T

139557371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469201-G-A

139557371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469201-G-T

http://identifiers.org/hco/4/GRCh38#139557373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51469203-C-A

139557425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469255-A-G

139557472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469302-C-T

http://identifiers.org/hco/4/GRCh38#139557491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51469321-C-A

139557491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469321-C-T

http://identifiers.org/hco/4/GRCh38#139557581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51469414-C-A

139557581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469414-C-T

http://identifiers.org/hco/4/GRCh38#139557602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51469435-C-A

139557602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51469435-C-T

http://identifiers.org/hco/4/GRCh38#139557651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51469477-C-A

139557651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51469477-C-G

http://identifiers.org/hco/4/GRCh38#139557658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51469484-C-A

139557774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51469974-G-T

139557791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51469991-G-A

139557862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51470067-G-A

139558263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51470940-C-T

139558644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51471305-G-A

139558718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51471360-C-T

139558794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron variant
orthologous variants: 51471428-G-A

139559326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51471850-G-A

139559349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51471870-C-T

139559355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51471892-G-T

139559390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51472006-C-T

139559391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51472007-G-A

139559391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51472007-G-C

139559460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472145-T-C

139559595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472275-C-T

http://identifiers.org/hco/4/GRCh38#139559638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51472318-C-A

139559853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472508-C-G

139559853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472508-C-T

139559909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472573-A-T

139559910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472574-T-A

139559910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51472574-T-C

139560163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51473432-T-C

139560168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51473437-G-A

139560544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51473824-T-C

139560558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51473836-A-G

139560612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51473896-G-A

139560615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51473899-G-A

139561121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51474369-T-C

139561121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51474369-T-G

139563073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51475820-C-T

139563127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51475877-T-A

139563173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51475923-G-A

139563173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51475923-G-T

139563212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51475960-G-A

139563660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51476341-G-A

139563804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51476439-G-T

139563850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51476487-T-C

139564134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51476746-T-A

139564139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51476751-G-A

139564800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51477962-A-G

139564925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51478110-G-T

139564992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51478181-A-G

139564992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51478181-A-T

139566177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479024-G-T

139566216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479065-A-G

139566318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479156-A-G

139566327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479165-C-G

139566327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479165-C-T

139566586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479435-G-A

139566628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479500-G-A

139566842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479719-T-C

139566985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51479859-T-C

http://identifiers.org/hco/4/GRCh38#139567419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51480250-C-A

139568284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51481131-C-T

http://identifiers.org/hco/4/GRCh38#139568312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51481173-C-A

139568433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51481253-A-G

139568496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51481316-G-A

139568496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51481316-G-C

http://identifiers.org/hco/4/GRCh38#139568505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51481325-C-A

139568640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51481443-G-C

139568642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51481445-G-A

http://identifiers.org/hco/4/GRCh38#139568655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#51481458-A-C

139568700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51481500-A-T

139568805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51481606-G-A

139568870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51481670-C-T

http://identifiers.org/hco/4/GRCh38#139574879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51484618-C-A

139574977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51484707-T-C

139575017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51484747-C-T

139575135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51484866-G-A

139575392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51485095-C-T

http://identifiers.org/hco/4/GRCh38#139575729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51485411-A-C

139575743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51485422-C-T

139575968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51485596-T-C

139576200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51485837-G-A

139576291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51485940-C-G

139576319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51485968-C-G

139576345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51485986-A-G

139577006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487164-G-A

139577018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487185-C-T

139577035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487202-C-G

139577035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487202-C-T

139577342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487413-A-G

139577376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487429-C-G

139577468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51487529-G-A

139577656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51488224-A-G

139577827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51488327-G-C

http://identifiers.org/hco/4/GRCh38#139580435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51490671-C-A

139580435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51490671-C-T

139580441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51490677-G-A

139580474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51490711-A-G

139583742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51491632-A-T

139583882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51491759-C-T

139585084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51493785-T-G

139585558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51494262-C-G

139585558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51494262-C-T

139585811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51494821-C-T

139585840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51494843-T-A

139585840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51494843-T-C

139586100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495033-A-T

139586101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495034-T-C

139586401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495312-T-C

139586440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495350-G-A

139586468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495378-G-T

139586473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495383-G-A

139586473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495383-G-C

139586719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51495621-G-C

139592706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51500767-G-A

139592752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51500822-G-T

139592778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51500844-G-A

139592855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51500920-T-C

139593086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51501105-A-G

139593700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51504350-A-T

139593899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51504544-T-G

139594400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51505068-C-T

139594447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51505113-G-T

http://identifiers.org/hco/4/GRCh38#139594468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51505135-A-C

139595006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506099-A-G

139595232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506251-C-G

139595245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506264-A-G

139595264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506283-C-T

139595461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506466-T-C

139595515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506510-C-T

139595540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506535-G-A

139595600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506598-T-C

139596276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506736-C-T

139596323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506776-G-A

139596340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51506793-G-A

139596537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51508097-T-A

http://identifiers.org/hco/4/GRCh38#139596701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51508254-A-C

http://identifiers.org/hco/4/GRCh38#139596810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51508333-C-A

139596810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51508333-C-T

139596847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51508371-A-G

139596972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51508479-G-T

139602908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511197-T-C

http://identifiers.org/hco/4/GRCh38#139602926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51511214-C-A

139603082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511377-C-G

139603151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511444-G-A

139603166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511458-G-A

139603267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511560-C-T

139603313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511605-A-G

139603502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51511997-T-C

139603683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51514090-G-A

139603797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51514179-A-G

http://identifiers.org/hco/4/GRCh38#139604113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#51514471-C-A

139604132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30412
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51514490-T-G