38646902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non coding transcript exon variant
orthologous variants: 90364793-G-A

38646957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non coding transcript exon variant
orthologous variants: 90364853-A-G

38647031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non coding transcript exon variant
orthologous variants: 90364928-G-A

38647050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non coding transcript exon variant
orthologous variants: 90364950-G-A

38647050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non coding transcript exon variant
orthologous variants: 90364950-G-T

http://identifiers.org/hco/12/GRCh38#38647351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90367307-C-A

38647351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367307-C-T

http://identifiers.org/hco/12/GRCh38#38647624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90367436-C-A

38647624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367436-C-T

38647689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367496-G-T

http://identifiers.org/hco/12/GRCh38#38647764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90367573-C-A

38647766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367575-A-G

38648008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367754-C-T

38648084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367816-G-A

38648175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367868-C-T

38648205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367898-T-A

38648205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90367898-T-C

38648628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90368253-T-A

38648766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90369900-G-C

38648766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90369900-G-T

38648965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90370087-A-G

38649016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90370139-G-A

38651446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90370930-G-A

38651447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90370931-G-T

38651806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90371184-T-C

38652127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90371463-T-C

38652186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90371510-G-A

38652260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90371587-T-C

38652497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90371819-G-T

38652832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372174-G-T

38652893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372235-G-A

38653063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372402-T-G

http://identifiers.org/hco/12/GRCh38#38653118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90372459-A-C

http://identifiers.org/hco/12/GRCh38#38653229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90372566-C-A

38653229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372566-C-T

38653236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372576-G-A

38653250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372590-A-G

38653267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372602-G-T

38653349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372647-T-A

38653360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90372657-G-A

http://identifiers.org/hco/12/GRCh38#38653407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90372704-C-A

38653436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372733-G-C

38653436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372733-G-T

38653472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372767-A-T

http://identifiers.org/hco/12/GRCh38#38653497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90372792-C-A

38653497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372792-C-T

38653498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372793-A-G

38653515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372810-G-T

38653519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372814-C-T

http://identifiers.org/hco/12/GRCh38#38653613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90372909-C-A

38653613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372909-C-T

38653628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90372924-A-T

38653999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90373307-A-G

38653999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90373307-A-T

38654062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90373370-T-C

38654092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90373399-G-C

38654149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90373458-A-G

http://identifiers.org/hco/12/GRCh38#38654514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90373924-C-A

38654546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90373949-T-A

http://identifiers.org/hco/12/GRCh38#38654555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90373958-C-A

38654555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90373958-C-G

38654555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90373958-C-T

38654718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90374128-C-T

38654791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90374200-C-T

http://identifiers.org/hco/12/GRCh38#38655383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90374669-C-A

38664716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90376458-A-G

38665104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90376826-T-G

38665711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90377440-T-C

38665888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90377577-A-T

38665929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90377610-A-G

38666080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90377772-T-C

http://identifiers.org/hco/12/GRCh38#38666192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90377871-A-C

38666586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378121-G-A

38666695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378208-A-T

38666728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378242-G-A

38667010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378491-A-G

38667040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378525-A-G

38667082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378567-C-G

38667217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378688-C-T

38667264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378740-T-C

38667266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378742-C-T

38667298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378782-A-G

38667492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90378944-A-G

38667622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90379070-C-T

38668159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90379302-T-C

38668234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90379355-G-C

38668234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90379355-G-T

http://identifiers.org/hco/12/GRCh38#38668639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90379720-C-A

38669281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380042-T-A

38669388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380187-G-A

38670173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380482-A-G

38670187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380496-G-A

http://identifiers.org/hco/12/GRCh38#38670231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90380540-C-A

http://identifiers.org/hco/12/GRCh38#38670270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90380583-C-A

38670302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380614-T-G

38670328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380649-C-T

38670332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380653-T-A

38670380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380693-T-A

38670380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380693-T-C

38670399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380712-G-A

38670511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380872-G-A

38670511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380872-G-T

38670577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380932-T-A

38670577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380932-T-G

http://identifiers.org/hco/12/GRCh38#38670582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90380937-C-A

38670582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380937-C-T

38670587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380942-T-A

38670587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380942-T-C

38670587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380942-T-G

38670607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380962-T-C

38670683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381008-T-C

38670684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381009-G-T

38670706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381031-G-T

http://identifiers.org/hco/12/GRCh38#38670823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90381368-A-C

38671022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381476-T-A

38671022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381476-T-C

38671033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381485-C-T

38671078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381508-G-A

38671085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381515-G-A

38671085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381515-G-T

http://identifiers.org/hco/12/GRCh38#38671101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90381540-A-C

38671244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381665-T-C

38671572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381947-G-T

38671719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90382060-A-G

38671816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90382154-G-A

38674019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90382697-G-C

38674257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90382924-T-C

38674260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90382927-T-C

38674619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383311-G-A

38674711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383365-A-G

38674718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383372-G-A

38674854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383423-A-G

http://identifiers.org/hco/12/GRCh38#38674961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90383472-A-C

38674961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383472-A-T

38675086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383551-T-C

38675125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383585-T-G

38675178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383610-C-T

38675425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383870-T-C

38675432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383877-G-C

38675485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90383927-C-T

http://identifiers.org/hco/12/GRCh38#38675618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90384015-C-A

38675622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90384019-T-A

38675622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90384019-T-G

38676144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90384318-A-T

38676233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90384386-T-A

38677306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385472-G-A

38677306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385472-G-T

38677425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385597-G-T

38677500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90385662-T-A

38677500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90385662-T-C

38677585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385751-A-G

38677600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385770-T-C

38677668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385825-T-C

38677691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385848-A-G

38678471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386832-T-C

38678533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386905-A-G

38678544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386914-T-C

http://identifiers.org/hco/12/GRCh38#38678606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90386976-C-A

38678795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90387091-C-T

38679197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90387399-C-T

38679533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90387661-T-C

38679543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90387663-T-C

38679587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90387705-T-G

http://identifiers.org/hco/12/GRCh38#38679682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90387784-A-C

38679836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90387902-A-G

38679959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90387997-G-C

38679992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90388017-T-A

38680193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90388217-A-G

http://identifiers.org/hco/12/GRCh38#38680288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90388309-A-C

38680602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90389111-C-T

38680651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90389183-C-T

38680711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90389243-G-C

38683473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390642-A-G

38683503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390672-G-A

38683509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390678-T-C

38683509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390678-T-G

http://identifiers.org/hco/12/GRCh38#38683651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90390821-A-C

38683651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390821-A-G

38683747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390910-T-C

38683927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90391439-T-C

38683952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90391467-T-C

38684212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90391731-G-A

38684854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392165-T-C

38685173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392471-C-T

38685349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393556-T-C

http://identifiers.org/hco/12/GRCh38#38685366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90393568-C-A

38685366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393568-C-G

38685366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393568-C-T

38685377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393579-G-T

38685398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393602-A-G

http://identifiers.org/hco/12/GRCh38#38685426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90393624-C-A

38685437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393635-G-T

38685472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393680-T-A

38685472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393680-T-C

http://identifiers.org/hco/12/GRCh38#38685669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90393876-C-A

38685680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90393887-T-C

http://identifiers.org/hco/12/GRCh38#38685706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90393911-A-C

38685706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393911-A-G

38685716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393921-T-C

38685784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393987-T-C

38685808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394003-T-C

38685809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394004-G-A

38685809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394004-G-C

38685926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394139-T-G

38685930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394143-T-A

http://identifiers.org/hco/12/GRCh38#38685992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90394204-C-A

38685992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394204-C-T

38686014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394224-G-A

38686014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394224-G-C

38686068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394290-T-C

38686192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394401-A-G

38686286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394490-C-T

38686510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394661-T-C

38688047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90397936-C-G

38688230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90398128-C-T

38688351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90398254-G-A

38688443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90398345-T-C

38690343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90398481-A-G

38690434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90398562-G-A

38690500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90398630-G-T

38690807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90398912-A-T

38690912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90398999-A-T

38692733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399246-T-G

38692775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399288-C-G

38692966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399464-G-A

38693002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399502-T-C

38693097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399569-C-T

http://identifiers.org/hco/12/GRCh38#38693343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90399809-C-A

38693343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399809-C-G

http://identifiers.org/hco/12/GRCh38#38693446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90399906-A-C

38693527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90399975-T-C

38693563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400016-G-T

38693566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400019-A-T

38693574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400026-G-A

38693574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400026-G-T

38693669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90400123-G-A

38693865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400318-A-G

38693905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400365-G-A

38693905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400365-G-T

38693911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400366-T-A

38693911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400366-T-C

38693923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400378-A-G

38696167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400414-C-G

38696251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400479-G-C

http://identifiers.org/hco/12/GRCh38#38696429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90400638-C-A

38696429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400638-C-T

38696498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400708-T-C

38696501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90400710-G-A

38702516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405857-C-T

38702560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405866-A-G

38702861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90406097-A-G

38702977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90406208-T-C

http://identifiers.org/hco/12/GRCh38#38703068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90406284-C-A

38705260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407388-C-T

38705310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407434-T-G

38705444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407554-A-G

38705646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407751-A-G

38705747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407835-A-G

38705787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407874-G-C

38705827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407912-C-G

38705827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90407912-C-T

38705952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90408003-C-T

38706931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90408903-G-A

http://identifiers.org/hco/12/GRCh38#38707455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90409551-A-C

38707467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90409563-A-G

38707473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90409569-G-A

http://identifiers.org/hco/12/GRCh38#38707676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90409774-C-A

38707740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90409825-T-C

38707835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90409920-C-T

38707928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410004-A-G

38707951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410027-T-A

38707987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410065-G-T

38708282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410276-A-G

38708299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410290-C-G

38708299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410290-C-T

38708421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410386-T-C

38708421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410386-T-G

38708448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410405-C-T

38708491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410416-T-C

38708491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410416-T-G

38708492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410417-G-A

38708583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410502-A-T

38708685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410590-G-A

38708711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410616-T-A

38708752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410622-G-A

38708794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410638-A-G

38708794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410638-A-T

http://identifiers.org/hco/12/GRCh38#38708976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90410780-C-A

38709121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90410877-T-C

http://identifiers.org/hco/12/GRCh38#38709259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90410980-C-A

38709318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90411029-T-C

38709318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90411029-T-G

38709363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90411076-C-T

38709788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90411668-C-G

http://identifiers.org/hco/12/GRCh38#38710294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90419344-C-A

38710356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90419421-G-A

38710410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90419465-A-T

http://identifiers.org/hco/12/GRCh38#38710467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90419529-A-C

38710504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90419566-G-A

38711327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90420269-C-T

38711362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90420301-G-T

38711884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90420615-G-A

38712813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422101-T-C

38712828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422116-A-G

38712883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422167-C-G

38712928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422213-A-G

38713040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422318-A-T

38713064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422340-A-G

38713076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422352-T-C

38713106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422382-T-G

38713369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90422599-G-A

http://identifiers.org/hco/12/GRCh38#38713395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90422620-A-C

38718508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423100-A-G

38718553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423136-G-T

38718564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423147-G-T

38718570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423153-G-C

38718584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423168-C-G

38718584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423168-C-T

38718594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423178-G-A

38718594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423178-G-T

38718676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423256-T-A

38718755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423312-C-T

38718760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423317-T-G

http://identifiers.org/hco/12/GRCh38#38718808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90423371-A-C

38718814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90423377-G-C

38723853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424539-A-G

38723869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424557-T-C

http://identifiers.org/hco/12/GRCh38#38723877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90424565-C-A

38723877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424565-C-G

38723877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424565-C-T

38723883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424581-T-C

38723888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424586-C-T

http://identifiers.org/hco/12/GRCh38#38723895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90424593-A-C

38723895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424593-A-G

38723901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424595-A-G

38723941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424635-A-G

38723964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424654-C-T

38723965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424655-T-C

38723987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424668-A-G

38724039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424724-A-G

38724143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424812-T-C

38724162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424829-A-G

http://identifiers.org/hco/12/GRCh38#38724179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90424846-C-A

38724329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90424981-C-T

38724362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425029-T-C

38724445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425125-G-A

38724504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425171-T-C

38724694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425327-T-C

38724729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425362-C-G

38724729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425362-C-T

http://identifiers.org/hco/12/GRCh38#38724739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90425372-C-A

38724784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425400-A-G

38724784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425400-A-T

38724817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425431-T-C

38724822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425436-T-A

38724822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425436-T-C

38724835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425449-A-G

38724858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90425472-A-G

38725011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425604-T-C

38725022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425615-A-G

http://identifiers.org/hco/12/GRCh38#38725037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90425631-C-A

38725037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425631-C-T

38725112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425706-A-G

38725136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90425729-G-C

38726618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90429821-T-C

38726678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90429880-G-A

http://identifiers.org/hco/12/GRCh38#38726702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90429890-C-A

38726724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90429907-G-A

38726758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90429937-A-G

38726933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430112-G-T

38727176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430327-T-C

38727237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430408-A-G

http://identifiers.org/hco/12/GRCh38#38727447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90430517-C-A

38727453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430523-G-A

38727552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430571-A-G

38727634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430653-G-T

38727641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90430660-G-T

http://identifiers.org/hco/12/GRCh38#38728953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90433479-C-A

38728953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433479-C-T

38728984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433510-T-A

38728984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433510-T-C

38729075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433602-T-C

38729319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433849-G-A

38729396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433921-A-T

38729421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90433944-T-C

38729522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434054-T-C

38729542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434084-G-C

38729701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434252-C-T

38729707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434258-C-G

38729854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434368-T-C

38729891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434405-T-G

38730021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434529-A-G

38730022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434530-G-A

38730022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90434530-G-C

38730263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90436157-T-C

38730263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90436157-T-G

38730307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90436201-C-T

http://identifiers.org/hco/12/GRCh38#38730380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90436277-A-C

38731343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437077-C-T

38731458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437183-C-T

38731508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437235-T-C

38731604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437331-C-G

38731667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437402-A-G

38731813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437533-T-C

38731936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437654-T-G

38731954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437672-C-G

38731956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437674-C-T

38732232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90437905-C-T

http://identifiers.org/hco/12/GRCh38#38732240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90437913-C-A

38732440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90438132-G-A

38732708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90438337-C-T

38732814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90438400-T-C

38733006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90438581-C-T

38733383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90439491-G-A

38733383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90439491-G-T

38733531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90439632-G-A

38733595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90439676-C-T

http://identifiers.org/hco/12/GRCh38#38734180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90440235-C-A

38734184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440239-C-G

http://identifiers.org/hco/12/GRCh38#38734298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90440462-C-A

38734298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440462-C-T

38734341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440497-T-C

38734346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440501-C-T

38734589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440687-A-T

38734635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440731-C-T

http://identifiers.org/hco/12/GRCh38#38734646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90440796-A-C

38734672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440991-T-C

38734673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90440992-G-A

38734692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90441011-C-T

38734755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90441071-T-A

38734894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90441216-T-C

38734910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90441234-C-T

38734957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90441272-C-T

38734984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90441300-T-C

38735677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90442529-T-C

http://identifiers.org/hco/12/GRCh38#38736202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90443044-C-A

38736202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90443044-C-T

38736219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90443062-A-G

38736219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90443062-A-T

38736320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90443195-A-T

38736398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90443261-T-C

38736503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90443350-A-G

http://identifiers.org/hco/12/GRCh38#38736542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90443385-A-C

38736968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90444134-T-C

38754332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90447853-T-C

38754422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90447911-T-C

38754656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448124-C-T

38754658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448126-T-C

38754658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448126-T-G

38754724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448196-T-C

38754912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448327-G-A

38754941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448356-T-C

38755256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448644-A-G

38755463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448851-C-T

38755533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448922-A-G

38755533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90448922-A-T

38755630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90449005-T-A

38755674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90449051-T-C

38755701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90449082-G-A

38756095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90449169-A-G

38756388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90449415-C-T

38757188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451313-G-A

38757204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451327-G-A

38757369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451440-T-C

38757453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451505-A-G

http://identifiers.org/hco/12/GRCh38#38757568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90451615-A-C

38757573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451620-G-A

38757573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451620-G-T

38757835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451867-T-C

38757872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451909-A-G

38757875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90451912-C-T

38760528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452126-T-C

38760627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452247-T-G

38760691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452303-C-T

http://identifiers.org/hco/12/GRCh38#38760745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90452358-A-C

38760745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452358-A-G

38760755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452368-T-A

38760786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452390-C-G

38760797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452408-C-T

38760837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452442-A-G

38760945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452576-G-A

38760945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452576-G-C

38760945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452576-G-T

38760971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452603-T-C

38761000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452631-G-C

38761010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452641-A-G

38761021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452671-G-T

38761210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452959-T-G

38761228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452976-A-G

38761240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90452988-T-C

38761256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90453004-A-G

38761510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90453210-T-C

http://identifiers.org/hco/12/GRCh38#38761518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90453229-C-A

38762013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90453562-T-G

38762043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90453586-A-G

38762109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90453660-T-C

38765104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90454328-G-A

38765217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90454447-G-T

38765454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90454671-G-A

38765475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90454692-A-G

38765561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90454752-T-C

38765689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90454877-A-T

38766245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90455097-T-C

38766701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90455360-T-G

38766910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90455546-T-A

38766973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90455582-T-C

38767354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90455900-A-G

38767489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456012-T-G

38767507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456029-A-G

38767507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456029-A-T

38767513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456035-A-G

38767575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456093-T-A

38767575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456093-T-C

http://identifiers.org/hco/12/GRCh38#38767596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90456115-C-A

38767596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456115-C-T

38767615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456128-T-C

38767616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456129-G-A

38767616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456129-G-T

38767620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456133-A-G

38767625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456138-A-G

38767742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90456255-A-G

38767797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456310-A-G

http://identifiers.org/hco/12/GRCh38#38767844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90456357-C-A

38767844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456357-C-T

38767951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456459-T-G

38768003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456508-G-A

38768046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90456551-T-C

http://identifiers.org/hco/12/GRCh38#38776191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90469036-A-C

38776191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90469036-A-G

38776231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90469074-T-A

38776231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90469074-T-C

38776316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90469159-A-G

38776317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90469160-T-C

38776339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90469193-T-A

38776339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90469193-T-C

http://identifiers.org/hco/12/GRCh38#38776432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90469275-A-C

38815582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90476059-T-C

38815665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90476145-G-C

38815719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90476199-T-C

http://identifiers.org/hco/12/GRCh38#38816020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90476366-C-A

http://identifiers.org/hco/12/GRCh38#38816385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90476778-A-C

38816543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90476928-G-A

38816543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90476928-G-C

http://identifiers.org/hco/12/GRCh38#38816544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90476929-C-A

38816600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90476985-A-G

38816667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477056-G-A

38816667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477056-G-T

38816718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477108-A-G

38816722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477112-T-C

http://identifiers.org/hco/12/GRCh38#38816816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90477202-A-C

38816828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477214-T-C

38821080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477651-C-G

38821080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477651-C-T

http://identifiers.org/hco/12/GRCh38#38821285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90477837-C-A

38821296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90477847-T-C

38821700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90478257-A-G

38821774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90478331-G-T

38821790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90478366-C-T

38821807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90478383-G-A

http://identifiers.org/hco/12/GRCh38#38821902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90478462-C-A

http://identifiers.org/hco/12/GRCh38#38821978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90478509-C-A

38822146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90478884-A-G

http://identifiers.org/hco/12/GRCh38#38822703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90479622-C-A

38822737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90479663-A-T

38822763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90479689-A-G

38823003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90480694-A-G

38823051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90480760-C-T

38823160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90480861-C-T

38823255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90480948-T-C

38823364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481055-T-G

38823557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481221-C-T

38823795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481429-T-G

38823821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481452-A-G

38823831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481462-A-T

38824237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481850-T-A

38824324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90481935-A-G

38824620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90482212-T-A

38824620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90482212-T-C

38824642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90482231-A-G

38824719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90482333-G-C

38825007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90482567-G-A

38825045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90482597-G-C

38825657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483179-T-C

http://identifiers.org/hco/12/GRCh38#38825709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90483228-C-A

38825739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483258-C-T

38825764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483284-G-A

38825827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483360-T-C

http://identifiers.org/hco/12/GRCh38#38825868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90483403-C-A

http://identifiers.org/hco/12/GRCh38#38826105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90483591-C-A

38826105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483591-C-T

38826107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483593-C-T

38826318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483778-T-C

38826417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483854-G-C

38826519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483925-G-A

38826570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483976-G-C

38826586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90483994-T-A

38826625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484033-T-C

38826749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484133-T-C

38826792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484170-T-C

38826829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484207-A-G

38828364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484863-G-A

38828364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484863-G-T

38828438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484934-C-T

38828449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90484945-T-C

38828534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90485029-T-C

38828553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90485049-G-A

http://identifiers.org/hco/12/GRCh38#38828647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90485129-A-C

http://identifiers.org/hco/12/GRCh38#38829147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90485785-C-A

38829579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486212-T-C

38830508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486390-G-T

38830564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486445-C-T

38830620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486492-C-G

http://identifiers.org/hco/12/GRCh38#38830771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90486664-C-A

38830952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486817-C-T

http://identifiers.org/hco/12/GRCh38#38830959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90486824-A-C

38831058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486912-C-G

38831058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486912-C-T

38831181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90486993-A-G

38831203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90487004-G-T

38831448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90487220-G-A

38831998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90487783-T-C

38832066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90487858-G-A

38832066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90487858-G-C

38832084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90487875-A-G

38832877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90490849-T-C

38832999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90490986-A-G

38833443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90491108-T-A

38833881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90492624-G-A

38833881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90492624-G-C

38833955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90492699-G-C

38834013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90492727-G-A

38834124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90492814-T-C

38834223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90492940-A-G

http://identifiers.org/hco/12/GRCh38#38834366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90493080-C-A

38834378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493092-A-G

38834378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493092-A-T

38834651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493344-C-T

38834743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493426-T-C

38834776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493458-A-G

38835679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493902-C-T

38835680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493903-T-C

38835761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90493988-A-G

38835886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90494117-G-C

38836194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90494382-A-G

38836235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90494423-C-T

38836467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90494938-G-C

http://identifiers.org/hco/12/GRCh38#38836527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90495001-C-A

38836527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495001-C-T

38836715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495187-C-T

http://identifiers.org/hco/12/GRCh38#38836779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90495249-C-A

38837010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495492-G-A

38837010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495492-G-T

38837297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495851-G-A

38837297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495851-G-T

38837331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90495918-C-T

38837556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90496205-G-A

38837610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90496256-T-A

38837610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90496256-T-C

38838030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90496968-C-T

38838689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90497953-T-C

38838985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90498211-A-G

38839290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90498795-T-A

38839334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90498841-G-A

38839407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90498880-A-G

38839424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90498892-G-A

38839556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90498999-C-G

38839569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499013-A-G

http://identifiers.org/hco/12/GRCh38#38839619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90499066-C-A

http://identifiers.org/hco/12/GRCh38#38839744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90499160-A-C

38839761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499177-T-C

38839940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90499338-T-C

http://identifiers.org/hco/12/GRCh38#38840024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90499418-C-A

38840024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499418-C-T

38840026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499420-A-G

38840044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499435-A-G

http://identifiers.org/hco/12/GRCh38#38840054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90499445-C-A

http://identifiers.org/hco/12/GRCh38#38840120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90499506-A-C

38840522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499606-T-C

38840642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499723-G-C

38840739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90499842-A-G

38845607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90501047-T-C

38845617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90501057-T-A

38845871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90501281-C-T

38846058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90501443-A-G

38846836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90501884-G-A

38847027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90502059-G-A

38847042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90502071-T-C

38847180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90502169-T-C

38847280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90502258-G-A

http://identifiers.org/hco/12/GRCh38#38847556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90502517-C-A

38847670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90502600-C-G

38847704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90502634-T-C

38848134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503207-C-T

38848201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503266-T-G

38848408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503468-G-C

38848408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503468-G-T

38848410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503470-G-T

38848466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503743-T-C

http://identifiers.org/hco/12/GRCh38#38848600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90503876-C-A

38848600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90503876-C-T

38848602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90503878-G-A

38848602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90503878-G-T

http://identifiers.org/hco/12/GRCh38#38848702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90503987-C-A

38848702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90503987-C-T

38848904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90504187-C-G

38848910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90504193-C-G

38849046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90504321-A-G

38849271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90504524-A-G

38849535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90504804-T-C

38850474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90508676-G-T

http://identifiers.org/hco/12/GRCh38#38850858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90509038-A-C

38850883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509062-T-C

38850902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509079-G-T

38850937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509095-T-C

38850942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509100-G-C

38851057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509171-A-G

http://identifiers.org/hco/12/GRCh38#38851176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90509273-C-A

38851176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509273-C-T

38851248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509348-A-G

38851501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509596-C-T

38851514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509609-C-G

38851545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509640-A-T

38851598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509690-A-T

38851612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90509704-C-T

http://identifiers.org/hco/12/GRCh38#38853803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90510401-C-A

38853869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90510464-A-G

38853869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90510464-A-T

38854100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90511066-G-A

38854100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90511066-G-C

38854259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90511342-A-G

38854270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90511353-G-A

38854287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90511370-A-G

38871783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90530070-C-T

38871816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90530087-T-C

38872179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532010-T-C

38872252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532088-G-A

http://identifiers.org/hco/12/GRCh38#38872262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90532098-A-C

38872342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532180-C-T

38872427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532265-G-T

http://identifiers.org/hco/12/GRCh38#38872464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90532284-C-A

38872487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532306-T-C

38872497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532316-A-G

38872536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532353-C-G

38872536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532353-C-T

38872685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532538-T-C

38872685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532538-T-G

38872908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532689-G-A

38872908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532689-G-T

38872926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532707-G-A

38872926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532707-G-T

http://identifiers.org/hco/12/GRCh38#38872957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90532735-C-A

38872957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532735-C-T

http://identifiers.org/hco/12/GRCh38#38873042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90532819-A-C

38873088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90532861-T-C

38873304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533017-G-A

http://identifiers.org/hco/12/GRCh38#38873329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90533058-A-C

38873387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533110-C-T

http://identifiers.org/hco/12/GRCh38#38873400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90533123-A-C

38873503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533212-G-C

38873541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533247-G-A

38873606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533311-C-T

38873640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533342-C-T

38874452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533424-G-A

38874452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533424-G-T

38874461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533433-A-G

38874826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90533734-C-T

38875830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90534843-C-T

38875948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90534955-G-A

http://identifiers.org/hco/12/GRCh38#38876161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90535151-A-C

38876173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90535163-C-G

38876702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90535260-T-G

38876717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90535275-C-G

38876807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90535358-G-A

38876855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90535405-G-C

38876967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90537386-A-G

38877237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90537643-C-T

38877341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90537793-T-C

http://identifiers.org/hco/12/GRCh38#38877445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90538034-C-A

http://identifiers.org/hco/12/GRCh38#38877597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90538182-C-A

38877597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90538182-C-T

38878348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90538616-G-A

http://identifiers.org/hco/12/GRCh38#38878490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90538756-C-A

http://identifiers.org/hco/12/GRCh38#38878627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90538897-A-C

38878633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90538903-G-T

38878714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90538967-C-T

38878743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90539005-T-C

38878772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90539034-T-C

38878847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90539106-T-A

http://identifiers.org/hco/12/GRCh38#38878872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90539139-A-C

38878988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90539253-C-T

38879646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90540321-C-T

38879656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90540331-T-C

http://identifiers.org/hco/12/GRCh38#38879686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90540350-C-A

38880139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90540729-T-C

38880205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90540783-T-A

38880312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90540881-G-A

38880354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90540919-C-T

38880653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90541124-A-G

38880665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90541136-T-G

38880702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90541155-C-T

38880746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90541177-T-G

http://identifiers.org/hco/12/GRCh38#38881175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90541509-A-C

38881257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90541605-G-C

38881711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90542001-A-G

38881765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90542040-G-C

38884032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90546560-C-T

38884038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90546566-T-C

38884096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90546617-T-G

38884414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90546951-G-A

38884429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90546956-G-A

38884435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90546962-C-T

38884523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90547039-A-G

38884554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90547070-C-G

38884670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90547168-T-C

38884742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90547222-T-C

38886053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90548177-G-T

38886080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90548192-G-A

38886115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90548228-G-T

38886143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90548257-C-T

38886811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550138-G-A

38886823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550150-T-C

38886960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550285-G-A

38886960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550285-G-C

38886961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550286-A-G

http://identifiers.org/hco/12/GRCh38#38887002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90550326-C-A

38887210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550516-T-C

38887233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550538-G-A

38887531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550750-T-G

38887694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90550961-C-G

38887734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90551009-T-A

38887769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90551044-G-A

38887781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90551055-A-T

38887795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90551067-A-G

38887948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90551198-T-C

38888372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90551577-G-T

http://identifiers.org/hco/12/GRCh38#38888789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90552101-A-C

38888807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552119-C-T

38888811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552123-A-G

38888957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552244-A-G

38888966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552251-A-G

38888970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552255-A-G

38889039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552323-C-T

38889356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552623-G-C

38889575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90552860-C-T

38889839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90553370-G-A

38889885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90553416-A-G

38890182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90553709-C-T

38890264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90553790-T-C

38890285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90553811-T-G

http://identifiers.org/hco/12/GRCh38#38890353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90553881-A-C

38890569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90554150-A-T

38890755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90554289-T-C

38890811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90554349-A-G

38890811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90554349-A-T

38892794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90557243-T-C

38892916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90557365-C-G

38894225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90558308-A-G

38894321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90558409-T-C

http://identifiers.org/hco/12/GRCh38#38894358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90558445-C-A

38894379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90558467-G-A

38900620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90559012-C-G

http://identifiers.org/hco/12/GRCh38#38900762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90559199-C-A

38901761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90560087-A-T

38902117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90560424-T-G

38903014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90561264-T-C

38903235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90561420-G-A

38903338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90561528-C-T

http://identifiers.org/hco/12/GRCh38#38903460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90561637-C-A

38903471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90561647-C-T

38903846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90561972-C-T

38903895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90562013-T-G

38905253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90563182-C-T

38905442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90563376-G-A

38905442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90563376-G-C

38905442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90563376-G-T

38905448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90563382-G-A

38905448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90563382-G-C

38905448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 90563382-G-T

http://identifiers.org/hco/12/GRCh38#38905477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#90563411-C-A

38905477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563411-C-T

38905526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90563460-G-A

38905526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90563460-G-T

38905548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563482-G-A

38905548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563482-G-T

38905549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563483-C-T

38905624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron variant
orthologous variants: 90563565-T-C

38905624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron variant
orthologous variants: 90563565-T-G

38905649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, undefined
orthologous variants: 90563590-G-A

38905649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, undefined
orthologous variants: 90563590-G-T

http://identifiers.org/hco/12/GRCh38#38905746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#90563672-C-A

38905746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563672-C-T

38905747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563673-T-A

38905768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563694-G-A

38905768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563694-G-C

38905768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563694-G-T

38905813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563725-G-A

38905813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563725-G-C

38905935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563745-G-A

38905994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563763-G-T

38906027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563784-T-A

38906027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90563784-T-G

http://identifiers.org/hco/12/GRCh38#38906168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90563816-C-A

http://identifiers.org/hco/12/GRCh38#38906289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#90563919-C-A

38906289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90563919-C-T

38906492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564096-A-G

38906536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564133-C-G

http://identifiers.org/hco/12/GRCh38#38906549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#90564145-C-A

38906549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564145-C-T

http://identifiers.org/hco/12/GRCh38#38906551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#90564147-C-A

38906551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564147-C-G

38906551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564147-C-T

38906581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564175-A-G

38906591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564186-G-A

38906591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 90564186-G-T

http://identifiers.org/hco/12/GRCh38#38906718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#90564285-A-C

38906718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564285-A-G

38906729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564293-T-C

38906729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564293-T-G

38906758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90564324-G-A

38906758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90564324-G-C

38906758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90564324-G-T

38906778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564348-A-G

38906806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564376-A-G

38906806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564376-A-T

38906814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564381-G-A

38906814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564381-G-C

38906814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564381-G-T

38906835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564391-T-A

38906844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 90564400-G-A

38906931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90564446-G-A

38907032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90564547-C-T

38907210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90564729-G-A

38907210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90564729-G-T

38907239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90564764-T-C

38907399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90564947-T-C

38907399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90564947-T-G

38907412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23498
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 90564958-T-C