38324595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97222960-C-T

http://identifiers.org/hco/17/GRCh38#38324599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97222964-C-A

38324599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97222964-C-G

38324599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97222964-C-T

38324613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97222966-C-G

38324613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97222966-C-T

38324641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97222991-G-C

38324641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97222991-G-T

38324727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223081-G-A

38324814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223172-G-A

38324814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223172-G-T

38324930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223274-G-A

38325028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223351-C-G

38325270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223584-A-G

38325338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223632-C-T

38325401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223692-G-A

38325401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223692-G-T

http://identifiers.org/hco/17/GRCh38#38325498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97223744-C-A

38325498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3 prime UTR variant
orthologous variants: 97223744-C-G

http://identifiers.org/hco/17/GRCh38#38325545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97223791-C-A

38325547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97223793-G-A

38325631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97223868-G-A

38325631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97223868-G-T

38325736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97223951-G-T

http://identifiers.org/hco/17/GRCh38#38325772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97223980-C-A

38325772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97223980-C-T

http://identifiers.org/hco/17/GRCh38#38325821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97224029-A-C

http://identifiers.org/hco/17/GRCh38#38325852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97224060-C-A

38325852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224060-C-G

38325870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224077-A-T

38326203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224890-G-A

38326203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224890-G-T

38326229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224916-T-C

38326245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224932-G-A

38326257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224944-G-T

38326285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224962-T-C

38326289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224966-G-A

38326289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224966-G-T

38326306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224977-T-C

38326309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224980-A-G

38326309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224980-A-T

38326311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224982-G-A

38326311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224982-G-C

38326311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97224982-G-T

38326341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97225010-G-C

38326341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97225010-G-T

38326368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97225036-A-G

38326380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97225048-T-C

38326407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97225075-G-A

38326407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97225075-G-T

38326475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225282-T-C

38326626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225436-G-C

http://identifiers.org/hco/17/GRCh38#38326645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97225452-A-C

38326645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97225452-A-G

38326656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225463-T-C

38326656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225463-T-G

38326676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225483-C-T

38326748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225555-G-A

http://identifiers.org/hco/17/GRCh38#38326840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97225644-A-C

38326840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97225644-A-G

38327079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225868-C-G

38327079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97225868-C-T

38327347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226079-C-T

38327397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226129-G-T

38327430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226162-T-C

38327442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226174-C-G

38327461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226193-A-G

38327580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226297-C-G

38327580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226297-C-T

http://identifiers.org/hco/17/GRCh38#38327589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97226306-C-A

38327589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226306-C-T

38327739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226456-T-C

38327794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226481-G-A

38327844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226543-C-T

38327967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 97226654-G-A

38327967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226654-G-C

38327974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226661-T-C

38327992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226679-T-C

38328091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226778-A-G

38328135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226822-T-G

38328136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226823-G-A

38328251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226932-G-A

38328251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97226932-G-C

38328274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226955-C-G

38328274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97226955-C-T

38328322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97227003-C-T

38328364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97227045-A-G

http://identifiers.org/hco/17/GRCh38#38328382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97227063-A-C

38328382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97227063-A-G

http://identifiers.org/hco/17/GRCh38#38328410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97227091-C-A

38328412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97227093-C-T

38328414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97227095-A-G

38328557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227190-G-A

38328559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227192-T-A

38328602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227223-G-T

38328681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227293-C-G

38328681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227293-C-T

38328696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227308-C-T

38328697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97227309-A-T

38328917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227523-T-C

http://identifiers.org/hco/17/GRCh38#38328922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97227528-A-C

38328935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227541-T-C

http://identifiers.org/hco/17/GRCh38#38329018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97227624-C-A

38329018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227624-C-G

http://identifiers.org/hco/17/GRCh38#38329071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#97227677-C-A

38329071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227677-C-T

38329081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97227687-C-T

38329085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227691-A-G

38329101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: stop gained
orthologous variants: 97227707-G-A

http://identifiers.org/hco/17/GRCh38#38329203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97227809-C-A

38329203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227809-C-G

38329305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97227902-C-G

38329424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228018-G-A

38329452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228046-G-A

38329520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228081-C-T

38329591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97228152-G-A

38329591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97228152-G-C

38329591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97228152-G-T

38329597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97228158-C-T

38329971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228541-G-A

38330000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228570-C-T

38330021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228591-A-G

38330170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97228740-G-A

38330170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97228740-G-T

38330365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97228935-G-C

38330459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229029-A-G

38330514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229084-G-A

38330533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97229103-G-C

38330535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229105-G-A

38330613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229183-G-A

http://identifiers.org/hco/17/GRCh38#38330625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97229195-A-C

http://identifiers.org/hco/17/GRCh38#38330666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97229236-A-C

38330666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229236-A-G

http://identifiers.org/hco/17/GRCh38#38330816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97229395-C-A

38330908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97229487-T-G

38331038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229620-G-A

38331038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229620-G-T

38331162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229747-T-C

38331295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97229880-G-A

38331295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97229880-G-T

38331337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97229922-G-A

38331337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97229922-G-C

38331340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97229925-G-A

38331421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97230006-G-A

38331434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97230019-C-T

38331538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 97230123-G-A

38331600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230180-C-G

38331600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230180-C-T

38331611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230198-T-C

38331636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230227-T-C

http://identifiers.org/hco/17/GRCh38#38331660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97230252-C-A

38331660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230252-C-T

http://identifiers.org/hco/17/GRCh38#38331663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97230255-C-A

38331675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230262-T-A

38331675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230262-T-C

38331679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97230266-A-G

38332403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97231402-C-G

38333238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97232153-G-A

38333296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97232211-G-A

38333341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97232256-G-A

38333412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97232330-T-A

38333418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97232336-T-A

38333418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97232336-T-G

38333490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97232366-G-T

38333652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97232486-T-C

38333746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233264-C-T

38333904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, undefined
orthologous variants: 97233385-A-G

38333924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233403-G-C

38333924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233403-G-T

38334070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233556-G-T

http://identifiers.org/hco/17/GRCh38#38334117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97233599-C-A

38334117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233599-C-G

http://identifiers.org/hco/17/GRCh38#38334130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97233618-C-A

38334130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233618-C-T

38334180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233662-G-A

38334180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233662-G-T

38334605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233968-G-T

38334607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233970-G-T

38334628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233991-G-T

38334630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233993-G-C

38334630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233993-G-T

38334631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97233994-G-T

38334645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234005-G-A

38334645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234005-G-C

38334645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234005-G-T

38334650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234010-G-A

38334650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234010-G-T

38334666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234026-G-C

38334701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234061-C-G

38334766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97234126-T-C

http://identifiers.org/hco/17/GRCh38#38334876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97234299-C-A

38334994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234398-G-A

38334994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234398-G-T

38335178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97234580-A-G

38335261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97234663-G-A

38335261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97234663-G-C

38335261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97234663-G-T

38335369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234742-T-C

38335466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234807-G-A

38335466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234807-G-C

38335466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234807-G-T

38335531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234865-G-A

38335531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234865-G-T

38335580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234912-C-G

38335580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97234912-C-T

38335656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97234988-A-G

38335659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97234991-G-A

38335659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense variant
orthologous variants: 97234991-G-C

38335671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97235003-T-C

38335723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235056-T-C

38335797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235126-A-G

http://identifiers.org/hco/17/GRCh38#38335811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97235139-C-A

38335828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235156-G-A

38335828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235156-G-C

38336013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235370-G-A

38336013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235370-G-T

38336014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235371-G-A

38336014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97235371-G-T

38336066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236524-A-G

38336185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236643-G-A

38336185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236643-G-T

38336190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236647-T-C

http://identifiers.org/hco/17/GRCh38#38336244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97236699-C-A

38336244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236699-C-T

http://identifiers.org/hco/17/GRCh38#38336270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97236725-C-A

38336270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236725-C-T

38336276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236729-G-A

38336276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236729-G-T

38336416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97236781-C-T

38336848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237179-T-C

38336859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237190-G-T

38336888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237217-A-T

38336946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237258-C-T

38337059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97237374-G-A

38337059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97237374-G-T

38337074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97237389-G-A

38337080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97237395-T-C

38337131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97237446-T-C

38337221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 97237536-G-T

38337236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237551-A-G

38337237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237552-G-A

38337237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237552-G-T

38337239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237554-G-A

38337239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237554-G-T

http://identifiers.org/hco/17/GRCh38#38337275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97237590-C-A

38337320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237623-T-A

38337320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237623-T-C

38337338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97237641-A-G

http://identifiers.org/hco/17/GRCh38#38337524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97238080-C-A

38337581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238179-C-T

38337629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238228-A-G

http://identifiers.org/hco/17/GRCh38#38337634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97238233-C-A

38337711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: synonymous variant
orthologous variants: 97238310-G-A

http://identifiers.org/hco/17/GRCh38#38337780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97238376-C-A

38337786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238382-G-A

38337787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238383-G-C

38337787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238383-G-T

38337866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238451-G-C

38337866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238451-G-T

http://identifiers.org/hco/17/GRCh38#38337905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97238489-C-A

38337999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238568-T-C

38338092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97238649-G-A

38338211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97239369-G-T

38338244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97239390-G-A

38338301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97239449-G-T

38338339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97239497-G-A

http://identifiers.org/hco/17/GRCh38#38338958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97239625-A-C

38339045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97239690-A-G

38339210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97240350-G-A

38339210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97240350-G-T

http://identifiers.org/hco/17/GRCh38#38339301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97240441-C-A

38339301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron variant
orthologous variants: 97240441-C-T

38339387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97240499-A-G

38339563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97240664-G-T

38341423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241004-T-C

38341471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241054-T-G

http://identifiers.org/hco/17/GRCh38#38341787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97241335-C-A

38342254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241443-C-T

38342875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241936-T-A

38342875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241936-T-C

http://identifiers.org/hco/17/GRCh38#38342922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97241981-C-A

38342922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241981-C-G

38342922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97241981-C-T

38342958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97242011-C-G

38342959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97242012-C-T

38343046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242099-T-C

38343046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242099-T-G

38343280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242333-C-T

38343330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97242383-G-T

38343385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242438-G-A

http://identifiers.org/hco/17/GRCh38#38343542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97242595-C-A

38343542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97242595-C-T

38343553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242606-G-C

38343559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97242612-A-T

38343579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242632-G-A

38343747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97242800-G-A

http://identifiers.org/hco/17/GRCh38#38343771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97242824-C-A

http://identifiers.org/hco/17/GRCh38#38343872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97242918-C-A

38343872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 5 prime UTR variant
orthologous variants: 97242918-C-T

http://identifiers.org/hco/17/GRCh38#38343900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97242949-C-A

38343912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 5 prime UTR variant
orthologous variants: 97242961-G-A

38343912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 5 prime UTR variant
orthologous variants: 97242961-G-C

38343912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31371
most severe consequence: 5 prime UTR variant
orthologous variants: 97242961-G-T