http://identifiers.org/hco/2/GRCh38#238848139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91729279-C-A

238848139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91729279-C-G

238848139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91729279-C-T

http://identifiers.org/hco/2/GRCh38#238848809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#91729930-C-A

238848809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 91729930-C-T

238848825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 91729946-G-A

238848825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 91729946-G-T

http://identifiers.org/hco/2/GRCh38#238848829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#91729950-C-A

238848865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91729985-T-A

238848865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91729985-T-G

http://identifiers.org/hco/2/GRCh38#238848868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91729988-C-A

238848868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91729988-C-G

238848868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91729988-C-T

238848913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730035-G-A

238849055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730169-G-T

238849091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730205-C-T

238849241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730306-A-T

238849468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730538-C-T

238849478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730548-C-G

238849591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730631-G-T

238849665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730722-G-C

238849729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91730770-C-T

238850344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91731377-G-T

http://identifiers.org/hco/2/GRCh38#238850433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91731465-C-A

238850546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91731576-T-C

238850613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91731646-T-A

238850613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91731646-T-C

238850710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91731742-G-C

http://identifiers.org/hco/2/GRCh38#238850879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91731887-A-C

238850879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91731887-A-G

238851308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91732274-G-C

238851321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91732287-A-G

http://identifiers.org/hco/2/GRCh38#238851569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91732533-C-A

238851569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91732533-C-T

238851648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91732840-T-G

238852369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91733472-G-A

238852414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91733516-A-T

238852417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91733519-C-T

238852707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91733833-G-A

238852898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734121-A-G

238852898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734121-A-T

238852961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734177-G-A

238852961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734177-G-C

http://identifiers.org/hco/2/GRCh38#238853235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91734431-A-C

238853235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734431-A-G

238853407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734558-G-C

238853557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734634-T-C

238853560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734637-T-C

238853647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734722-A-G

238853874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734952-G-A

238853876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734954-G-A

238853876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91734954-G-C

238853974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91735036-G-A

238854191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91735233-A-G

238854499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91735466-C-T

238854858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736196-T-G

238855049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736365-T-A

238855078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736390-C-G

238855078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736390-C-T

238855086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736400-T-G

238855094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736414-C-T

238855211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736533-A-G

238855354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736692-A-G

238855358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736696-G-T

238855512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91736863-T-C

238855730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91737050-A-G

http://identifiers.org/hco/2/GRCh38#238855859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91737169-C-A

238856162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91737459-G-T

238856297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91737572-A-G

http://identifiers.org/hco/2/GRCh38#238856610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91737857-A-C

238856610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91737857-A-G

238856948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738361-C-T

238856982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738395-C-T

238856995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738408-G-A

238857008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738425-C-T

238857354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738641-G-A

http://identifiers.org/hco/2/GRCh38#238857363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91738650-A-C

238857436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738726-G-T

238857610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738843-C-T

238858072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91738922-T-G

238858275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739118-C-T

238858391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739232-T-C

238858788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739605-C-T

238858800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739617-C-T

238858850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739678-C-T

238859251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739759-C-T

238859274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739785-C-T

238859279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91739790-C-T

238859969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91740212-T-G

238860006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91740249-C-T

238863082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743153-A-G

238863082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743153-A-T

238863215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743276-G-A

238863263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743366-C-T

238863451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743567-C-T

238863455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743571-G-A

238863455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743571-G-T

238863484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743618-C-T

238863725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91743893-G-A

238864086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91744245-G-A

238864086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91744245-G-T

238864324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91744481-G-C

238864369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91744526-C-G

238864579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91744722-G-T

238864598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91744744-C-T

238865927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91746707-C-T

http://identifiers.org/hco/2/GRCh38#238865932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91746712-C-A

238865932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91746712-C-T

238866049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91746771-G-C

238866148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91746864-C-T

238867603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747247-G-A

238867690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747351-G-A

238867783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747434-A-G

238867829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747459-G-C

238868060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747642-A-G

238868212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747780-T-A

238868362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91747915-T-C

238868608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748104-C-T

238868641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748136-G-A

238868841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748292-C-T

238868885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748351-C-T

238869037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748485-G-A

238869154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748575-G-C

http://identifiers.org/hco/2/GRCh38#238869221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91748635-C-A

238869226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748640-G-A

238869243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748657-C-T

238869258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748672-T-G

238869399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748816-A-G

238869526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91748979-A-G

238869609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91749048-T-C

238875037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91750785-C-G

238875175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91750902-T-G

http://identifiers.org/hco/2/GRCh38#238875330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91751042-C-A

238875477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91751184-T-C

238875732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91751408-G-A

238875941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91751604-C-T

238876045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91751697-G-A

238876573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91752777-C-T

238876622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91752831-T-G

238876683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91752892-G-C

238876804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91753023-A-G

238877474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91753931-A-G

238877540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754000-A-G

238877735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754148-C-T

238877746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754159-T-A

238877746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754159-T-C

238877944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754342-C-T

238878013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754408-G-A

238878076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754464-G-C

238878210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754546-C-T

238878234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754570-C-G

238878234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754570-C-T

238878327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754627-C-T

238878405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754704-C-T

238878406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754705-G-A

238878449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754756-A-G

238878563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754863-G-A

238878667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91754957-G-T

238878805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91755094-G-A

238878858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91755125-C-T

238878970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91755226-G-A

238879112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91755348-T-C

http://identifiers.org/hco/2/GRCh38#238882428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91756866-C-A

238882453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91756889-G-C

http://identifiers.org/hco/2/GRCh38#238883287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91758116-A-C

238883287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758116-A-G

238883349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758184-A-T

http://identifiers.org/hco/2/GRCh38#238883827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91758646-A-C

238883907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758720-G-A

238884043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758792-C-T

238884157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758865-G-C

238884218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758914-T-C

238884243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91758942-C-G

238884568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91759198-A-G

238884605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91759238-C-G

238884895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91759389-C-T

238884896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91759390-C-T

238884944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91759437-G-A

238885311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91759765-G-A

238886208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91760049-C-G

http://identifiers.org/hco/2/GRCh38#238886264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91760130-C-A

238886449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91760293-T-G

238887746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91760915-C-G

238887746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91760915-C-T

238887754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91760923-C-T

238887881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91761041-T-C

238887889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91761050-C-T

238887944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91761102-C-T

238887951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91761109-C-T

238888941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762071-T-C

238888978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762107-G-A

238888978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762107-G-T

238889025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762149-G-C

238889025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762149-G-T

238889096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762241-C-G

238889363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91762528-T-A

238889570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763013-C-T

238889576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763019-A-G

238889630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763072-T-C

238889665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763107-T-C

238889669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763111-T-C

238889709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763158-G-A

238889726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763175-G-T

238889732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763181-G-A

238889750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763199-C-T

238889777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763213-G-A

238889927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763355-G-A

238889929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763357-C-G

238889981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763399-G-A

238890173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763538-G-A

238890280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763651-G-A

238890490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763802-T-G

238890614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91763930-C-T

238894981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765614-G-T

238894989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765619-C-T

238895004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765633-C-G

238895009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765638-T-C

238895063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765693-G-A

238895108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765729-T-C

238895186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765797-G-C

238895209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765828-G-A

238895318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91765886-C-T

238895583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766140-G-A

238895690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766225-G-A

238895834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766355-G-A

238895868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766392-C-T

http://identifiers.org/hco/2/GRCh38#238895922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91766440-C-A

http://identifiers.org/hco/2/GRCh38#238896051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91766497-C-A

238896051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766497-C-T

238896105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766529-G-A

238896146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766567-G-A

238896146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766567-G-C

238896146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766567-G-T

238896147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766568-G-C

238896147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766568-G-T

http://identifiers.org/hco/2/GRCh38#238896298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#91766682-A-C

238896350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, undefined
orthologous variants: 91766708-G-C

238896350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, undefined
orthologous variants: 91766708-G-T

238896391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766745-C-T

238896806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766997-A-G

238896806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91766997-A-T

238897208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767368-C-T

238897244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767383-T-C

238897312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767435-C-T

238897344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767475-A-G

238897371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767504-C-T

238897572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767711-C-T

238897595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767735-C-T

238897668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91767811-A-G

238897951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91768062-A-G

238898152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91768201-G-A

http://identifiers.org/hco/2/GRCh38#238898351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91768412-A-C

238904569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91771989-A-G

238904588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91772014-G-A

238904604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91772030-G-T

238905233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91772424-G-A

238905446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91772595-G-T

238905843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91772983-G-A

238905919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, undefined
orthologous variants: 91773048-A-G

238905936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91773065-T-C

238905943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91773072-G-A

238905948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron_variant, undefined
orthologous variants: 91773077-C-T

238906057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91773158-T-A

238906060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91773161-A-G

238907470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91773753-G-A

238907470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91773753-G-T

238907652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91774105-A-G

238907739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91774195-C-T

238907812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91774260-C-G

238907812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91774260-C-T

http://identifiers.org/hco/2/GRCh38#238907890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91774323-C-A

238907890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91774323-C-T

238909703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91774989-A-G

238909723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91775009-G-T

http://identifiers.org/hco/2/GRCh38#238909724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91775010-C-A

238909724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: 91775010-C-T

http://identifiers.org/hco/2/GRCh38#238909823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91775092-C-A

http://identifiers.org/hco/2/GRCh38#238909917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91775185-C-A

238909917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 3 prime UTR variant
orthologous variants: 91775185-C-T

238910373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 3 prime UTR variant
orthologous variants: 91775593-T-C

238910390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20670
most severe consequence: 3 prime UTR variant
orthologous variants: 91775611-G-T