http://identifiers.org/hco/3/GRCh38#170459605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31256751-C-A

170459605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31256751-C-T

http://identifiers.org/hco/3/GRCh38#170460293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31257452-C-A

170460332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31257484-G-T

170460351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31257503-A-G

http://identifiers.org/hco/3/GRCh38#170460596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31257742-C-A

http://identifiers.org/hco/3/GRCh38#170460658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31257802-C-A

170460658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31257802-C-T

170460784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31257928-A-G

http://identifiers.org/hco/3/GRCh38#170460826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31257971-C-A

170460896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258037-G-A

170460896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258037-G-T

http://identifiers.org/hco/3/GRCh38#170461316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31258393-C-A

170461316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258393-C-T

http://identifiers.org/hco/3/GRCh38#170461394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31258469-C-A

170461582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258645-G-T

http://identifiers.org/hco/3/GRCh38#170461601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31258668-C-A

170461642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258703-G-T

170461643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258704-G-T

170461644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258705-G-A

170461644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258705-G-T

170461672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258733-A-G

http://identifiers.org/hco/3/GRCh38#170461714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31258778-C-A

170461714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258778-C-G

http://identifiers.org/hco/3/GRCh38#170461791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31258854-C-A

170461811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258874-G-A

170461811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258874-G-C

170461811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258874-G-T

170461912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258968-G-A

170461912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258968-G-T

170461913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258969-G-A

170461913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258969-G-T

170461945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31258990-C-G

http://identifiers.org/hco/3/GRCh38#170461955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31259000-C-A

170461970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259015-G-C

170461970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259015-G-T

170462003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259047-A-G

http://identifiers.org/hco/3/GRCh38#170462027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31259071-C-A

170462027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259071-C-T

http://identifiers.org/hco/3/GRCh38#170462047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31259087-C-A

170462047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259087-C-T

170462056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259095-G-A

170462056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259095-G-C

170462056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259095-G-T

170462090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259126-T-C

170462147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259170-G-T

http://identifiers.org/hco/3/GRCh38#170462192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31259204-C-A

170462201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259213-A-T

170462204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259216-G-A

170462204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259216-G-T

170462207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259219-G-C

170462239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259253-T-G

170462280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259301-G-A

170462382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259367-C-G

170462439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31259407-T-C

170464257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31260660-C-T

170464588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31260914-G-A

170464610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31260937-A-G

170464646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31260967-G-A

170464646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31260967-G-T

170464651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31260972-A-G

170464703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261024-G-A

170464708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261029-G-T

http://identifiers.org/hco/3/GRCh38#170464801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31261124-C-A

http://identifiers.org/hco/3/GRCh38#170465095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31261397-C-A

170465191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261477-G-T

170465492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261724-G-T

170465495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261727-T-C

170465509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261741-G-A

170465815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31261958-A-G

http://identifiers.org/hco/3/GRCh38#170466004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31262133-C-A

http://identifiers.org/hco/3/GRCh38#170466006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31262135-C-A

170466006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262135-C-G

170466017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31262146-A-G

170466080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262206-T-C

http://identifiers.org/hco/3/GRCh38#170466346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31262489-C-A

170466346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262489-C-G

170466410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262555-T-C

170466423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262568-G-A

170466446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262591-T-C

170466575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262712-G-A

http://identifiers.org/hco/3/GRCh38#170466675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31262837-C-A

170466675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262837-C-G

170466675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262837-C-T

http://identifiers.org/hco/3/GRCh38#170466682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31262853-C-A

170466682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262853-C-T

170466739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31262920-A-G

http://identifiers.org/hco/3/GRCh38#170466903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31263076-C-A

170466903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31263076-C-T

170466945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31263118-G-A

170466948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31263121-A-G

170467142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31263312-T-C

170467235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31263405-T-C

170467235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31263405-T-G

170467241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31263411-G-A

170467241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 31263411-G-C

170467241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 31263411-G-T

170467313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31263483-C-T

170467426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263593-T-A

170467426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263593-T-C

http://identifiers.org/hco/3/GRCh38#170467447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31263614-C-A

170467447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263614-C-G

170467447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263614-C-T

http://identifiers.org/hco/3/GRCh38#170467470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31263629-C-A

170467470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263629-C-G

170467470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263629-C-T

170467525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263660-G-C

170467525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31263660-G-T

170468014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265336-C-G

170468014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265336-C-T

170468237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31265565-T-C

170469195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31266701-G-T

170469315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31266821-A-T

170469421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31266923-A-G

170469474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31266977-G-T

170469565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31267075-T-A

170469642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31267146-G-A

http://identifiers.org/hco/3/GRCh38#170470149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31267611-C-A

170470572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31267905-T-A

170470683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268012-G-A

170470683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268012-G-T

170470822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268138-C-T

170470938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268250-A-T

170471118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268389-T-A

170471120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268391-T-A

170471122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31268393-A-T

170472992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31271402-A-G

170473032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31271439-A-G

170473080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31271486-G-T

170473522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31271944-C-T

http://identifiers.org/hco/3/GRCh38#170473614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31272037-C-A

170473619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272042-A-G

170473664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272082-T-A

170473685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272103-A-T

170473816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272235-C-T

170473967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272329-C-T

http://identifiers.org/hco/3/GRCh38#170473973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31272335-A-C

170474042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272409-A-G

170474043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272410-C-G

170474076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272440-A-G

170474080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272444-A-G

170474085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272449-A-G

170474116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272474-T-C

170474116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31272474-T-G

170474350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31272621-G-C

170474470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31272745-C-T

170474816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31273326-A-G

http://identifiers.org/hco/3/GRCh38#170474829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31273339-A-C

http://identifiers.org/hco/3/GRCh38#170474870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31273387-C-A

170474920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31273443-A-G

170475070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31273584-A-G

170475082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31273600-C-G

170475210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31273708-T-G

170475296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31273792-G-A

170475597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274112-A-G

170476534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274349-G-A

170476843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274605-G-T

http://identifiers.org/hco/3/GRCh38#170476844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31274606-A-C

http://identifiers.org/hco/3/GRCh38#170476868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31274630-C-A

170476910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274640-G-A

170476910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274640-G-C

170476910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274640-G-T

http://identifiers.org/hco/3/GRCh38#170476911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31274641-C-A

170476911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274641-C-T

170476917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274647-G-A

170476923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31274653-C-G

170477290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275015-G-C

170477386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275187-G-A

170477433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275236-T-G

170477712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275715-G-A

170477834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275840-T-C

170477834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275840-T-G

170477841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275847-A-G

170477858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31275864-T-C

170477925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31275924-G-A

170477961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31275954-C-T

http://identifiers.org/hco/3/GRCh38#170478462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31276115-C-A

170479943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31277278-C-T

170480180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31277513-A-G

170480180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31277513-A-T

http://identifiers.org/hco/3/GRCh38#170480305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31277627-C-A

170480305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31277627-C-G

170480305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31277627-C-T

http://identifiers.org/hco/3/GRCh38#170480449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31277771-C-A

170480449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31277771-C-G

170480449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31277771-C-T

http://identifiers.org/hco/3/GRCh38#170480469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31277791-C-A

170480491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31277813-G-A

170480608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31277930-T-C

170480716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31278038-A-G

170480776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31278098-T-C

170480776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31278098-T-G

170480908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31278230-G-A

170480989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31278311-G-A

170480989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 31278311-G-T

http://identifiers.org/hco/3/GRCh38#170481037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31278359-C-A

170481037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31278359-C-T

http://identifiers.org/hco/3/GRCh38#170481251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31278577-A-C

http://identifiers.org/hco/3/GRCh38#170481269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31278595-A-C

170481903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31279374-G-A

170482221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280017-G-A

170482389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280199-T-G

170482399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280209-A-G

170482403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280211-A-G

170482405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280213-G-A

170482445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280256-C-T

170482503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280314-G-T

170482540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280364-C-T

170482800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280738-C-G

170482975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31280902-C-T

170483085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281011-G-C

170483085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281011-G-T

170483202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281112-G-A

170483208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281118-G-T

http://identifiers.org/hco/3/GRCh38#170483361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31281241-C-A

170483361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31281241-C-G

170483361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31281241-C-T

170483367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31281247-G-A

170483403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31281283-C-T

170483546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281424-G-A

170483556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281434-C-G

170483556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281434-C-T

170483568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281446-A-G

170483569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281447-G-A

170483569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281447-G-C

170483619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281474-G-T

http://identifiers.org/hco/3/GRCh38#170483649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#31281503-C-A

170483649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281503-C-T

170483661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31281516-T-C

170483692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281543-T-C

170483792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281655-A-G

170483919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281822-C-G

170483919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281822-C-T

170483976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281877-C-T

http://identifiers.org/hco/3/GRCh38#170484024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31281920-C-A

170484024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31281920-C-T

170484605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31282284-G-C

http://identifiers.org/hco/3/GRCh38#170484733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31282403-C-A

http://identifiers.org/hco/3/GRCh38#170484765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31282435-C-A

170484765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31282435-C-T

170484771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31282441-T-C

170484957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31282631-T-C

170485170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31282845-G-C

170485557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31283363-T-C

170485816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31283599-C-T

170485948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31283729-C-T

http://identifiers.org/hco/3/GRCh38#170486209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31284416-A-C

170486209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284416-A-G

170486234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31284441-T-C

http://identifiers.org/hco/3/GRCh38#170486306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31284513-A-C

170486385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284592-A-G

170486429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284635-G-C

170486477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284683-A-G

170486482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284692-G-A

170486482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284692-G-C

170486482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31284692-G-T

http://identifiers.org/hco/3/GRCh38#170486895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31285083-C-A

170486918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285106-A-G

170487071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285210-A-G

170487199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285341-G-T

170487331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285471-G-T

170487419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285548-G-A

170487567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285640-C-T

170487687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285767-A-G

170487727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285805-T-G

170487847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285902-G-A

170487954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31285986-T-G

170488086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31286903-A-G

170488305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31287084-T-G

http://identifiers.org/hco/3/GRCh38#170488314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31287093-A-C

170488314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31287093-A-G

170493146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31288051-G-A

170493617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31288499-C-G

170493617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31288499-C-T

170493636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31288516-C-T

170493976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31288848-G-A

170494272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31289098-A-G

170494430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31289264-A-G

170494631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31289461-G-C

170494987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31289859-G-A

170495030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31289908-G-A

170495057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31289935-G-A

170497375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31290372-A-G

170497510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31290503-C-T

170497731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31290723-A-G

170498282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291198-T-A

170498282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291198-T-C

170498601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291468-T-A

170498601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291468-T-C

170498641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291492-A-G

170498736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31291587-G-A

170498736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31291587-G-C

170498736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31291587-G-T

170498813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31291664-G-C

170498832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31291683-G-A

170498832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31291683-G-C

170498838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31291689-C-T

170498959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291794-T-A

http://identifiers.org/hco/3/GRCh38#170498964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31291799-C-A

170499464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31291978-T-A

170499511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292029-T-C

170499616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292133-A-G

170499617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292134-T-C

170499632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292149-T-C

http://identifiers.org/hco/3/GRCh38#170499737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#31292260-C-A

170499737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31292260-C-T

170499784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292307-A-G

170501050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292687-C-G

170501078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292714-T-C

170501079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292715-G-A

170501100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31292734-C-T

http://identifiers.org/hco/3/GRCh38#170501147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31292781-C-A

170501147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31292781-C-T

170501167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31292801-T-C

170501169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31292803-G-A

170501169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 31292803-G-C

170501206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31292840-C-T

170501344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 31292978-G-A

170501344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 31292978-G-T

170501387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31293020-T-C

170501387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31293020-T-G

http://identifiers.org/hco/3/GRCh38#170501434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31293065-C-A

170501434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31293065-C-G

170501434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31293065-C-T

http://identifiers.org/hco/3/GRCh38#170501458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31293089-C-A

170501458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31293089-C-T

170501663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31294407-G-T

170501798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31294535-T-C

170508537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31297846-A-G

170508627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31297923-C-T

170508745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298032-G-A

170508745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298032-G-C

170508828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298112-C-T

170508934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298213-C-T

170509001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298279-G-C

http://identifiers.org/hco/3/GRCh38#170509392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31298673-C-A

170509392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298673-C-T

170510600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298933-C-T

170510609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31298942-A-G

170510697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31299016-G-A

170511470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31299048-G-C

170511484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31299062-A-G

170511763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31299300-C-T

170512245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31299766-G-A

170512362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31299879-A-G

170512583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300083-T-G

170512982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300421-G-A

170513008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300446-G-A

170513072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300488-G-C

170513072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300488-G-T

170513080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300496-G-A

170513080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300496-G-T

170513277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31300686-C-T

170513566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302164-G-A

170513636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302267-G-A

170513636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302267-G-T

170513671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302329-G-A

170513776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302437-C-T

170513787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302448-C-T

170513831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302490-A-G

170513958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302589-T-A

170514014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302637-C-T

170514127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302747-C-T

http://identifiers.org/hco/3/GRCh38#170514142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31302762-C-A

170514142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302762-C-T

170514210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31302819-T-C

170514922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31303261-G-T

http://identifiers.org/hco/3/GRCh38#170515321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31303395-A-C

170515321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31303395-A-T

http://identifiers.org/hco/3/GRCh38#170515323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31303397-A-C

170515323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31303397-A-G

170515610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31303641-G-T

170515798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31303814-G-A

170515914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31303928-T-A

http://identifiers.org/hco/3/GRCh38#170516040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31304049-C-A

170516224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31304222-C-T

170517952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31305906-T-G

170518215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31306138-C-G

170521077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31306876-G-T

170521360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31307174-A-G

170521582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31307443-A-G

170523393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31308097-C-T

170523476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31308175-T-G

http://identifiers.org/hco/3/GRCh38#170523503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#31308219-C-A

170523503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31308219-C-T

170523831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31308537-A-G

http://identifiers.org/hco/3/GRCh38#170523980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31308669-C-A

170524071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31308759-T-C

170524130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31308810-T-A

170524281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31308944-C-T

170524353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31309015-C-T

170524378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31309040-A-T

170524426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31309076-G-T

170524529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31309170-G-A

http://identifiers.org/hco/3/GRCh38#170524893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31309898-A-C

170524939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31309926-C-T

170525076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31310063-T-C

170525286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31310245-G-A

170526572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31311659-G-A

170526572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31311659-G-C

170526572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31311659-G-T

http://identifiers.org/hco/3/GRCh38#170526582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31311666-C-A

170526582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31311666-C-T

170526613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31311697-C-T

170526619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31311703-A-G

170526673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31311755-A-G

170526781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31311863-T-C

170526826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31311908-C-T

170526856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31311938-T-A

170526856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 31311938-T-C

170526981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31312065-G-A

170526981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31312065-G-C

170526981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31312065-G-T

http://identifiers.org/hco/3/GRCh38#170527140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31312220-C-A

170527204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31312280-T-G

170527511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31312959-A-G

170527714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313134-G-A

170527734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313158-G-A

170527740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313164-A-G

170527964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313422-G-A

170528029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313474-G-A

170528029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313474-G-T

170528396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31313749-A-G

170528618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31314092-C-G

170531770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316238-A-G

170531945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316397-G-C

http://identifiers.org/hco/3/GRCh38#170532085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31316508-A-C

170532085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316508-A-G

170532299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316706-G-A

170532549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316897-A-G

170532586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316927-T-C

170532697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316994-C-G

170532697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31316994-C-T

170532720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31317009-C-G

http://identifiers.org/hco/3/GRCh38#170532767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31317056-C-A

170532861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31317128-T-C

170533766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31318945-A-G

170533766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31318945-A-T

170534154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319324-T-G

170534182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319352-A-G

170534397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319531-G-A

http://identifiers.org/hco/3/GRCh38#170534460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31319621-A-C

170534542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319775-G-A

170534566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319799-G-A

170534573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319811-T-C

170534624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319884-T-C

170534625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319885-C-G

170534627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31319887-G-A

170534888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320157-T-C

170534892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320161-G-A

http://identifiers.org/hco/3/GRCh38#170535157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31320381-C-A

170535237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320448-A-T

170535261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320461-A-G

170535304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320496-G-T

170535686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320870-C-T

170535734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320929-T-G

http://identifiers.org/hco/3/GRCh38#170535753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31320960-C-A

170535753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320960-C-G

170535785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320988-C-G

170535785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31320988-C-T

170537207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31321525-A-G

http://identifiers.org/hco/3/GRCh38#170537221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31321539-C-A

170537221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31321539-C-G

170537736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31322194-G-A

170537786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31322244-T-A

170537986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323240-T-C

170538019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323280-G-A

170538135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323387-A-G

170538222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323459-A-G

170538609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323804-T-A

170538615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323810-C-T

170538752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323977-G-A

170538752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31323977-G-T

170538841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31324033-G-T

170539157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31324291-A-G

170539434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31324737-G-A

170539442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31324745-A-G

170539511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31324848-T-A

170539531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31324868-T-C

170540406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31325680-A-G

170540431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31325712-T-C

http://identifiers.org/hco/3/GRCh38#170541900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31326921-A-C

170541928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31326950-A-G

170541984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31327017-C-T

170542019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31327052-T-G

170542403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31327272-C-T

170542485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31327339-C-G

170542661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31327459-A-G

170544097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328386-C-T

170544126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328415-T-G

170544172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328464-C-T

170544277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328563-G-A

170544375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328638-C-G

170544375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328638-C-T

170544751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31328922-A-G

170544878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31329050-C-G

170544979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31329133-A-G

170545541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31330628-T-G

170545597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31330682-A-T

170545821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31330890-T-C

http://identifiers.org/hco/3/GRCh38#170545885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31330953-C-A

170545885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31330953-C-T

170545908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31330975-C-T

170545992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31331023-G-T

170546195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31331204-A-G

170546221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31331231-T-A

170546225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31331235-G-A

170546330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31331327-T-C

http://identifiers.org/hco/3/GRCh38#170548304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31332421-C-A

170548304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31332421-C-T

http://identifiers.org/hco/3/GRCh38#170548605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31332631-C-A

170548605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31332631-C-T

170548631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31332658-G-C

170549211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333218-C-G

170549211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333218-C-T

170549241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333248-A-G

170549241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333248-A-T

170549307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333305-C-T

170549308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333306-G-A

170549709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31333679-G-T

170550297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31334213-A-G

170550391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31334266-G-A

170550471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31334344-T-C

http://identifiers.org/hco/3/GRCh38#170550489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31334362-A-C

170550836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31334622-T-G

170550906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31334672-A-G

170551257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31334999-C-G

170551278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31335020-T-G

170551387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31335204-C-T

170551758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31335699-A-G

170551758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31335699-A-T

http://identifiers.org/hco/3/GRCh38#170551990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31335886-C-A

170553618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31336337-G-A

170553793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337074-C-T

170553807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337088-G-C

170553864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337133-G-A

170553864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337133-G-T

170553868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337138-G-T

170553887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337162-A-T

http://identifiers.org/hco/3/GRCh38#170554117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31337378-C-A

170554183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337430-C-T

170554254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337499-A-G

170554732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31337771-A-G

170556569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31338372-C-T

170556587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31338390-T-A

170556618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31338422-G-A

http://identifiers.org/hco/3/GRCh38#170557522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31340953-A-C

170557542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31340973-T-C

170557871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341297-A-G

170557937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341350-G-T

170558160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341531-G-A

170558283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341628-G-A

170558283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341628-G-T

170558327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341673-T-C

170558384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341728-A-G

170558504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31341817-G-T

170558905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31342186-C-T

170558917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31342198-A-G

170558936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31342217-T-G

170559036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31342319-A-G

170559217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343053-A-G

170559228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343062-T-C

170559285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343126-A-G

170559548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31343377-G-A

170563136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345586-T-C

170563136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345586-T-G

170563147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345597-G-C

http://identifiers.org/hco/3/GRCh38#170563185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31345636-C-A

170563188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345639-C-T

170563777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345877-C-T

170563900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31345982-T-C

170564289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346330-T-C

http://identifiers.org/hco/3/GRCh38#170564332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31346366-C-A

170564453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31346481-C-G

170565412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347092-G-A

170565412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347092-G-C

170565533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347204-G-T

170565693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347362-A-G

170565757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347427-C-G

170565766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347433-T-G

170565773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347440-C-G

170565972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347615-T-C

170566387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31347990-G-A

170566583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31348132-C-T

170566585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31348134-C-T

http://identifiers.org/hco/3/GRCh38#170566646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31348210-C-A

170566658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31348237-G-T

170566715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31348375-T-C

http://identifiers.org/hco/3/GRCh38#170566819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31348478-A-C

170571072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31350397-A-T

170571343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31350607-T-G

170571389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31350655-G-A

170571389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31350655-G-C

170571687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31350894-T-A

170571687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31350894-T-C

170572142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31351016-G-C

170572260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31351119-A-T

170572372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31351225-C-T

170572511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31351366-A-T

170572757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31351703-C-T

170572758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31351704-G-A

170572984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31351936-T-A

http://identifiers.org/hco/3/GRCh38#170573207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31352157-C-A

170573207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31352157-C-G

http://identifiers.org/hco/3/GRCh38#170573235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31352185-C-A

170573235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31352185-C-G

170574293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353127-T-G

170574541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353329-T-C

170574638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353429-T-A

170574828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353605-G-T

170574911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353688-C-T

170574981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353758-G-T

170574992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353769-G-A

170575188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353962-A-G

170575197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353971-G-T

170575203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31353977-T-C

170575287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354056-G-A

170575287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354056-G-T

170575621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354370-A-G

170575905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354613-A-G

170575942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354652-A-T

170575951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354663-A-G

http://identifiers.org/hco/3/GRCh38#170575966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31354681-C-A

170575966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354681-C-G

170576030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354730-T-C

170576278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31354906-C-T

http://identifiers.org/hco/3/GRCh38#170576361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31354977-A-C

http://identifiers.org/hco/3/GRCh38#170576399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31355013-A-C

170576527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31355401-T-A

170576614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31355479-C-G

170576721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31355575-G-T

170576743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31355596-C-T

170579333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357411-A-G

170579438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357511-T-A

170579438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357511-T-G

170579531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357611-T-C

170579611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357693-C-G

170579611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357693-C-T

170579652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357734-T-G

170579744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357818-C-G

170579746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357820-A-G

170579765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357838-A-G

170579909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31357987-T-C

170580045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31358121-T-C

170580083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31358689-G-A

170580364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31358980-C-T

170580374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31358990-G-A

170580446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359060-G-A

170580630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359235-A-G

170580753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359413-T-G

170580774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359432-T-C

170580860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359601-T-C

170580961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359691-T-C

170580971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359701-C-T

http://identifiers.org/hco/3/GRCh38#170581159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31359815-C-A

170581191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359847-G-T

http://identifiers.org/hco/3/GRCh38#170581299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31359950-C-A

170581330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31359978-G-A

http://identifiers.org/hco/3/GRCh38#170581528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31360132-A-C

170581564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31360169-G-A

170581626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31360218-T-G

170581628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31360220-A-G

170581682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31360277-T-C

170581760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31360351-A-G

170581805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31360394-G-T

170582466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361021-T-A

170582488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361043-A-G

170582597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361140-A-G

170582652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361199-A-G

170582817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361344-A-G

170582989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361534-T-C

170583007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361552-C-T

170583012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361557-A-G

http://identifiers.org/hco/3/GRCh38#170583022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31361567-A-C

170583022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361567-A-G

170583151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361691-G-A

170583151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361691-G-C

170583406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361913-T-A

170583439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361919-C-T

170583475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361954-T-C

170583493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31361972-A-G

http://identifiers.org/hco/3/GRCh38#170583896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31362362-A-C

170584154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31362631-T-C

170584289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31362764-G-A

170584289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31362764-G-C

170584289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31362764-G-T

170584328-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31362807-T-G

170584589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31363069-C-T

170585186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363625-G-C

170585186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363625-G-T

170585305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363737-G-C

170585322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363754-G-A

170585358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363789-C-T

http://identifiers.org/hco/3/GRCh38#170585390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31363820-A-C

http://identifiers.org/hco/3/GRCh38#170585428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31363859-C-A

170585432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363863-C-T

170585486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31363921-C-T

170585595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364030-G-A

170585595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364030-G-T

170585608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364044-T-C

170585621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364057-G-T

170585737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364163-C-T

170585765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364191-G-T

http://identifiers.org/hco/3/GRCh38#170585791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31364217-C-A

170585838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31364246-G-T

170585946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31364351-A-G

170585967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 31364372-C-T

170585992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31364378-T-C

170586032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31364417-G-A

170586032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31364417-G-T

170586036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31364421-G-A

170586036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 31364421-G-T

http://identifiers.org/hco/3/GRCh38#170586046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#31364431-C-A

170586046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31364431-C-G

170586046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29326
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31364431-C-T