43120869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94411200-T-A

43120869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94411200-T-C

43121216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: non coding transcript exon variant
orthologous variants: 94410868-G-A

43121216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: non coding transcript exon variant
orthologous variants: 94410868-G-T

43121296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: non coding transcript exon variant
orthologous variants: 94410789-C-T

43121312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: non coding transcript exon variant
orthologous variants: 94410772-T-C

43121807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409927-G-C

43121855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409875-A-G

43121922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409818-A-G

43121953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409780-C-G

43121953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409780-C-T

43121994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409706-C-T

43122063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409617-G-A

43122166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409552-G-A

43122202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409513-T-C

43122235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409486-C-T

43122236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409485-C-T

43122314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409407-A-G

43122483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409257-T-C

http://identifiers.org/hco/11/GRCh38#43122868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94408827-C-A

43122996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94408711-T-A

43123002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94408705-G-A

http://identifiers.org/hco/11/GRCh38#43123240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94408281-A-C

http://identifiers.org/hco/11/GRCh38#43123480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94408068-C-A

http://identifiers.org/hco/11/GRCh38#43123638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94407921-C-A

43124506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404940-A-G

43124506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404940-A-T

43124540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404907-C-T

http://identifiers.org/hco/11/GRCh38#43124542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94404905-C-A

43124542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404905-C-T

43124624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404837-T-C

43125038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404438-C-G

43125038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404438-C-T

43125163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404324-C-T

43126484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404286-T-C

43126496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404274-C-G

43127701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404192-C-G

43127727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404167-C-G

43127727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404167-C-T

43127792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404093-T-A

43127792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404093-T-G

43127793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404092-A-G

http://identifiers.org/hco/11/GRCh38#43127923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94403970-A-C

43127971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403911-T-C

43127981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403902-G-T

43127985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403898-A-G

43128399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403479-C-T

43128526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94403357-T-C

43130238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402722-A-T

http://identifiers.org/hco/11/GRCh38#43130354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94402613-C-A

43130365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402602-C-G

http://identifiers.org/hco/11/GRCh38#43130370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94402597-C-A

43130370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402597-C-T

43172693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401911-C-T

43172694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401910-G-A

43172992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399833-G-A

43173014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399811-G-C

43173142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399685-C-T

43173216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399611-A-G

43173231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399466-C-G

43173231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399466-C-T

43173345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399360-A-T

http://identifiers.org/hco/11/GRCh38#43174679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94399166-C-A

43174766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94399064-C-T

43174848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398986-T-C

43175249-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398421-T-A

43175488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94398055-T-C

http://identifiers.org/hco/11/GRCh38#43175797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94397606-C-A

43176008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397379-C-T

43176134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397251-C-T

http://identifiers.org/hco/11/GRCh38#43177788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94386787-C-A

43177894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386682-A-G

43177936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386641-C-T

43178042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386534-T-C

http://identifiers.org/hco/11/GRCh38#43178564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94386018-C-A

43178972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385522-C-T

43179013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385476-G-A

43179013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385476-G-C

43179046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385451-C-T

43179553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385395-G-A

43179692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385279-C-T

43179803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385135-T-C

43179839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385097-G-A

43179933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94385005-A-T

43179941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94384980-T-A

43179941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94384980-T-G

43180067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94384859-G-A

43180453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94383582-A-G

43180834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94383186-G-T

http://identifiers.org/hco/11/GRCh38#43180863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94383157-C-A

http://identifiers.org/hco/11/GRCh38#43181276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94382772-A-C

43181276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94382772-A-G

http://identifiers.org/hco/11/GRCh38#43181322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94382726-C-A

43181623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94382431-G-A

43181625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94382429-G-A

43181626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94382428-G-A

43181731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94382324-G-A

43181764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94382255-A-T

http://identifiers.org/hco/11/GRCh38#43182067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94382004-C-A

43182105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381970-G-A

43182110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381965-A-G

43182215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381850-T-C

43182226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381839-G-A

43182256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381817-A-G

43182279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381794-G-A

43182305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381769-G-C

43182537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381578-G-A

43182565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381550-A-G

43182588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381527-G-C

43182704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381427-G-T

43182926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381220-C-G

43182926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94381220-C-T

43183062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380740-C-T

43183087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380715-G-A

43183167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380640-T-A

43183292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380483-G-A

http://identifiers.org/hco/11/GRCh38#43183344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94380433-A-C

43183344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380433-A-G

43183358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380417-G-A

43183377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380398-A-T

43183457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380322-G-A

43183477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380304-G-A

43183687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379933-A-G

http://identifiers.org/hco/11/GRCh38#43183721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94379869-C-A

43183751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379839-C-T

43183788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379808-A-G

43183933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94379670-C-T

http://identifiers.org/hco/11/GRCh38#43184758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94379436-A-C

43185912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94371882-G-A

43186366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370533-G-C

43186489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370412-C-T

http://identifiers.org/hco/11/GRCh38#43186560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94370343-C-A

43187459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94367925-G-A

43189178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94366121-T-G

43189211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94366090-G-C

43189366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365944-G-A

43189508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365781-G-A

43190116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365320-T-A

43190117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365319-T-G

43190427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365007-T-C

http://identifiers.org/hco/11/GRCh38#43191582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94364863-C-A

43191742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364704-C-T

http://identifiers.org/hco/11/GRCh38#43191856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94364599-A-C

43192455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363954-A-G

43192472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363938-C-G

43192472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363938-C-T

43194834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362925-G-A

43197147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94362384-A-T

http://identifiers.org/hco/11/GRCh38#43197427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94362089-A-C

43197470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94362046-G-C

43197572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94361945-C-T

http://identifiers.org/hco/11/GRCh38#43197932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94361604-A-C

43197952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361584-A-T

43198295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94361272-A-T

43198875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360310-T-C

http://identifiers.org/hco/11/GRCh38#43199103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94360078-C-A

43199103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360078-C-T

43199131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360051-G-A

43199131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94360051-G-T

43199261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359930-A-G

43199535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359665-C-G

43199734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358636-A-G

43199744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358626-A-G

43199832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358540-A-G

43199944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358429-T-C

43200269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358155-T-C

43200269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358155-T-G

43213903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355780-A-T

43213921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355762-T-G

43214269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355422-A-G

43214345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355338-G-A

43214458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355272-A-G

43214526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355207-T-C

http://identifiers.org/hco/11/GRCh38#43214578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94355155-C-A

http://identifiers.org/hco/11/GRCh38#43214661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94355074-C-A

http://identifiers.org/hco/11/GRCh38#43214684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94355051-C-A

43214684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355051-C-G

43214738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355030-A-T

43214849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354950-C-G

43214908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354885-T-C

43215150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351629-A-G

43216110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349473-G-A

43216110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349473-G-C

43216211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349370-T-G

43216213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349368-A-T

43216337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349260-G-A

43216565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349024-C-T

43216773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348865-T-C

43217659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347883-T-C

43217911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347628-G-A

43217912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347627-C-T

http://identifiers.org/hco/11/GRCh38#43218596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94345588-C-A

43218596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345588-C-G

43218616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345565-T-G

43218758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345355-G-A

43218982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345130-C-T

43221312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345062-T-C

http://identifiers.org/hco/11/GRCh38#43221405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94344978-C-A

http://identifiers.org/hco/11/GRCh38#43222242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94344757-C-A

43222242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344757-C-T

43222700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344263-T-C

43223186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343818-G-A

43223186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343818-G-T

43223914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94342646-A-G

43224034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94342533-A-G

43224156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94342426-G-A

43224434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94342187-A-G

43224618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94342038-C-T

43224628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94342028-T-C

43224748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341916-T-C

43224758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341905-A-G

43225017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341669-G-A

43225116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341603-G-A

43225131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341588-G-A

43225259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341470-A-G

43225309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341431-C-T

43226046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94340751-C-G

43226069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94340728-G-C

43226416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94340213-A-T

43226417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94340212-T-G

43227237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94339424-A-G

43227237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94339424-A-T

43229946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94339085-C-T

http://identifiers.org/hco/11/GRCh38#43229957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94339074-C-A

43230384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94338513-A-T

43231377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94338095-T-A

43231377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94338095-T-G

43231404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94338068-T-C

43231413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94338059-G-C

43231413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94338059-G-T

43232072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94337409-C-T

43232308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94337154-G-A

http://identifiers.org/hco/11/GRCh38#43232311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94337151-C-A

43232311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94337151-C-G

43232369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94337005-T-G

43232407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94336959-T-C

43232671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94336651-A-T

43232688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94336633-C-T

43232760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94336559-A-T

43234100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94324526-A-G

http://identifiers.org/hco/11/GRCh38#43234106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94324532-C-A

43234106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94324532-C-T

43234178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94324596-T-C

43234272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94324768-T-C

43234917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325411-A-G

http://identifiers.org/hco/11/GRCh38#43234976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94325468-A-C

43234976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325468-A-G

43235232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325729-G-A

43235360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325853-C-T

43235368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325861-G-A

http://identifiers.org/hco/11/GRCh38#43235372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94325865-C-A

http://identifiers.org/hco/11/GRCh38#43235447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94325939-C-A

43235447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325939-C-T

43235464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94325952-C-T

http://identifiers.org/hco/11/GRCh38#43235465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94325953-A-C

43235669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326027-C-G

43235891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326240-G-A

43235995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326341-G-A

43236033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326372-G-A

43236033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326372-G-T

43236287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326635-C-T

http://identifiers.org/hco/11/GRCh38#43239925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94326667-A-C

43239925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326667-A-G

43239944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326686-T-G

43240044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94326774-C-T

http://identifiers.org/hco/11/GRCh38#43240775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94328138-A-C

43240789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328150-A-G

43240804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328161-A-G

43240891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328238-A-G

43241069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328427-G-T

43241078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328436-A-G

43243597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328626-T-C

43243633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328662-C-T

43243778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94328798-G-A

http://identifiers.org/hco/11/GRCh38#43243968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94328977-A-C

43244169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94329175-G-A

43244216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94329217-C-T

43244283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94329254-A-T

43244491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94329410-G-T

43244688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330332-A-T

43244698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330342-T-A

43244822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330445-G-A

43244822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330445-G-T

43244993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330607-C-T

43245013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330720-C-T

43245146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330863-C-T

43245167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94330884-A-G

43248031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94333139-A-G

43248295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94332829-T-G

http://identifiers.org/hco/11/GRCh38#43249263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94332531-C-A

43249286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94332508-C-T

43249307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94332487-C-T

43249815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94332001-T-C

43249882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94331933-T-A

43249960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94331843-A-T

43249984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94331817-A-G

43250048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94331684-G-C

43250103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94331622-T-A

43250829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94320511-C-T

http://identifiers.org/hco/11/GRCh38#43251010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94320362-A-C

http://identifiers.org/hco/11/GRCh38#43251455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94319953-C-A

http://identifiers.org/hco/11/GRCh38#43251468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94319940-A-C

43251468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319940-A-G

43251468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319940-A-T

43251565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319843-C-G

43251750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319696-A-G

http://identifiers.org/hco/11/GRCh38#43251811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94319622-A-C

43251812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319621-T-C

43251852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319524-A-T

43252101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319187-G-A

43252101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319187-G-T

43252109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319179-T-A

43252109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319179-T-C

43252109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94319179-T-G

43252460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94318845-G-A

http://identifiers.org/hco/11/GRCh38#43252988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94318354-C-A

43253086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94318269-G-A

43253232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94318129-T-C

43253389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317989-G-A

43253422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317956-T-A

43253709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317686-C-G

43253745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317652-C-T

http://identifiers.org/hco/11/GRCh38#43253845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94317546-A-C

43253845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317546-A-T

43254014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317297-C-G

43254087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317238-C-G

43254145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94317190-A-G

http://identifiers.org/hco/11/GRCh38#43263726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94316482-C-A

43263726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94316482-C-G

43263800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94316434-T-C

43264225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94316010-G-T

43264449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94315805-A-G

43264573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94315702-T-G

43264598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94315678-C-G

43265487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94314789-C-T

http://identifiers.org/hco/11/GRCh38#43265889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94314382-C-A

http://identifiers.org/hco/11/GRCh38#43266719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94313629-A-C

43266745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94313601-G-A

43266997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312177-G-A

43267071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312099-A-T

43267072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312098-T-G

43267082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94312083-C-T

43267286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311774-T-C

43267696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311206-T-A

43267696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94311206-T-G

43268039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310906-A-G

43268118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310814-A-G

43268137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310795-C-T

http://identifiers.org/hco/11/GRCh38#43268480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#94310464-C-A

43268516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310427-G-C

43268560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310383-G-C

43268785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310169-G-A

43268785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94310169-G-T

43269211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94309273-C-T

43269344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42376
most severe consequence: non coding transcript exon variant
orthologous variants: 94309185-T-C