157076271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 80820846-G-A

157076494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80820705-A-G

157076535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 80820686-G-T

157077005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80820364-T-A

157077005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80820364-T-G

157077035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80820337-G-T

157077213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80820142-T-A

157077365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819994-T-A

157077473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819901-T-G

157077741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819646-A-G

157077846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819544-T-C

157077886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819528-G-A

157077932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819486-A-T

157078133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 80819286-T-C

http://identifiers.org/hco/4/GRCh38#157078225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80819195-C-A

157078225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819195-C-T

http://identifiers.org/hco/4/GRCh38#157078240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80819180-C-A

157078240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819180-C-G

157078240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819180-C-T

157078287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819134-A-G

http://identifiers.org/hco/4/GRCh38#157078395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80819058-C-A

http://identifiers.org/hco/4/GRCh38#157078405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80819048-A-C

157078433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80819020-A-T

157078463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818995-A-G

157078463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818995-A-T

157078472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818986-T-C

157078630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818833-T-C

157079105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818651-T-C

157079201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818550-G-A

157079297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818469-G-A

157079574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818228-G-T

157079634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818183-C-T

157079754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80818072-T-A

157079927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817932-G-A

157079927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817932-G-C

157079986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817854-A-G

157080044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817803-A-T

157080060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817787-C-T

157080135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817708-A-G

157080250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817606-T-A

157080364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817487-A-G

157080377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80817474-G-T

157080631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80816914-G-A

157080810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80816757-G-T

157080955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80816607-A-G

http://identifiers.org/hco/4/GRCh38#157081534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80816162-C-A

157081556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80816143-C-G

157081679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80815986-C-T

157081696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80815959-C-T

157081706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80815927-T-C

157082001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80815666-T-G

157082140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80815521-G-C

157082515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80813216-G-A

157082792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812980-A-G

157082796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812976-G-A

157082885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812886-G-A

157082989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812739-T-C

http://identifiers.org/hco/4/GRCh38#157082993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80812735-C-A

157082993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812735-C-T

157083003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812725-C-T

157083114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812427-C-T

157083189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812356-G-A

157083200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80812345-T-C

157084371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80810158-C-T

157084438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80810087-T-A

157084472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80810052-T-C

157084526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80810004-A-G

http://identifiers.org/hco/4/GRCh38#157084721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80809816-A-C

157084724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 80809813-G-A

157084754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809794-T-A

157084754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809794-T-C

157084811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809742-T-C

157084811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809742-T-G

http://identifiers.org/hco/4/GRCh38#157084819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80809734-C-A

157084881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809662-C-T

157084898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809645-G-T

157084967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809578-T-C

157084974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809571-A-G

157085114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809398-G-A

157085193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809311-A-G

157086203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809006-G-A

157086208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80809001-T-A

157086496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808703-G-T

157086518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808681-G-A

157086646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808544-A-G

157086718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808473-G-A

157086730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808461-G-C

157086737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808454-T-C

157087165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80808052-A-T

157090364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80807265-G-A

http://identifiers.org/hco/4/GRCh38#157090504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80807131-A-C

157090588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80807049-C-T

157115844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80791440-G-T

157115882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80791408-T-C

157116047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80791236-T-A

157116158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80791128-A-G

157116180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80791106-C-T

157116237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80791049-T-C

157116253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80791032-G-T

157116375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80790921-A-T

157116418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80790892-A-G

157117187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80790169-C-G

157117195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80790161-A-G

http://identifiers.org/hco/4/GRCh38#157118514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80788338-C-A

157118640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80788209-T-C

http://identifiers.org/hco/4/GRCh38#157118760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80788108-A-C

157119274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80787621-A-T

http://identifiers.org/hco/4/GRCh38#157119587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80787265-A-C

157119587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80787265-A-T

157120487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80787120-A-G

157120566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 80787027-G-A

157120787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786837-T-C

157121092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786522-T-G

157121406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786278-C-T

157121440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786244-A-G

157121563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786106-G-A

157121563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786106-G-T

http://identifiers.org/hco/4/GRCh38#157121583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80786080-A-C

157121583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80786080-A-G

http://identifiers.org/hco/4/GRCh38#157122079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80785622-C-A

157122229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785477-T-G

157122231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785475-G-A

157122231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785475-G-T

http://identifiers.org/hco/4/GRCh38#157122255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80785451-C-A

157122255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785451-C-T

http://identifiers.org/hco/4/GRCh38#157122295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80785415-C-A

157122295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785415-C-T

157122426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785285-T-A

157122426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785285-T-C

157122485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785229-A-G

157122512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785201-T-C

157122668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80785062-G-C

157122853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80784486-A-G

157123254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80784147-A-G

157123389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80783994-C-G

157123443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80783946-G-A

157123651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80783750-G-C

http://identifiers.org/hco/4/GRCh38#157123780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80783592-C-A

157123887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80783485-T-C

157125058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80783157-A-G

http://identifiers.org/hco/4/GRCh38#157125080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80783139-C-A

157125168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80783058-G-T

157125319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782920-G-A

http://identifiers.org/hco/4/GRCh38#157125967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80782605-A-C

http://identifiers.org/hco/4/GRCh38#157126055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80782518-C-A

157126055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782518-C-G

157126055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782518-C-T

157126493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782071-G-A

157126493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782071-G-T

157126510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782054-C-G

157126510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80782054-C-T

157126677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781891-T-C

157126778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781793-T-G

157126792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781779-T-G

157126851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781721-A-G

157126856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781716-A-G

157126985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781592-T-G

http://identifiers.org/hco/4/GRCh38#157127197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80781368-A-C

157127197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80781368-A-G

157127717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80780790-T-G

157127783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80780723-G-T

157127786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 80780720-G-A

157127814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80780697-C-T

157128653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80779568-G-A

157128659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80779562-T-C

157129075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80779108-T-G

157129265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80778921-G-C

157129559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80778643-A-G

157129559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80778643-A-T

157129680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80778521-G-A

157133885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80773432-A-T

157134015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80773321-A-G

157134815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80772848-C-T

157134816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80772847-A-T

157134855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80772809-T-A

157135022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 80772666-C-T

157136452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 80769447-A-G

157136577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80769318-A-G

157136622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80769273-G-A

http://identifiers.org/hco/4/GRCh38#157136748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80769147-C-A

157137005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80768928-A-G

157137179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80768766-G-T

157137292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80768666-C-T

157137328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80768635-C-T

157137487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80768490-A-G

157138410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80767972-C-T

157138411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80767971-A-G

157138463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80767921-T-C

157138532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80767873-G-T

157138859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80767556-G-A

157138859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 80767556-G-T

157138958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767457-T-C

157138993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767418-T-C

157138994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767417-A-G

157139011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767399-T-C

http://identifiers.org/hco/4/GRCh38#157139050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80767371-A-C

157139050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767371-A-T

157139397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767030-C-G

157139418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80767009-T-C

157139528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766908-A-T

157139585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766856-G-A

157139771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766673-A-T

157139981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766558-G-A

157140049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766481-A-G

157141102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766331-G-T

157141151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766287-A-G

157141254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80766185-G-T

157141534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80765919-G-A

157141763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80765698-A-G

157141905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80765567-T-A

157142178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80765139-A-G

157142180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80765137-A-G

157142397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80764967-G-T

157142449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80764917-T-C

157142556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80764818-A-G

157142704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80764691-C-T

157143041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80763928-T-A

157143570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80763448-G-T

157143601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron_variant, undefined
orthologous variants: 80763418-C-T

157143703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron_variant, undefined
orthologous variants: 80763336-A-G

157143735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80763310-A-G

http://identifiers.org/hco/4/GRCh38#157143778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80763271-C-A

157143778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80763271-C-T

157143790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80763259-G-A

157143809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 80763240-T-G

157144061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80762283-T-A

157144131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80762211-T-C

157144263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80762080-G-A

157144570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80761592-G-A

157144570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80761592-G-T

157144655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80761504-T-G

157144674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80761494-G-A

157144674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80761494-G-T

157144808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80761400-C-T

157152006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80759199-G-C

157152022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80759184-G-A

157152052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80759156-C-T

157152088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80759121-A-G

157152154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80759016-G-A

157152171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758999-T-C

157152417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758755-A-G

157152467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758710-A-G

157152581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758607-T-G

157152592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758596-G-A

157152592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758596-G-C

157152592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758596-G-T

157152596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758592-A-G

157152657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758557-T-A

157152657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758557-T-C

157152701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758520-T-C

http://identifiers.org/hco/4/GRCh38#157153029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80758195-C-A

157153060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758166-T-C

http://identifiers.org/hco/4/GRCh38#157153125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80758117-C-A

http://identifiers.org/hco/4/GRCh38#157153145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80758097-C-A

157153145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758097-C-G

157153145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758097-C-T

157153160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80758082-T-C

157153431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80757850-C-G

157153440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80757841-T-C

http://identifiers.org/hco/4/GRCh38#157153569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80757711-C-A

157153569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80757711-C-T

http://identifiers.org/hco/4/GRCh38#157153606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80757675-C-A

157153615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80757666-C-T

157153733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80757551-G-A

157153758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80757526-A-G

157165216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754704-G-A

157165241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754677-G-A

157165298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754626-A-G

157165342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754578-T-C

157165355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754565-A-G

157165518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754400-A-T

http://identifiers.org/hco/4/GRCh38#157165619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80754308-A-C

157165654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754264-G-C

157165680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754236-T-C

157165844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754077-T-C

157165851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80754070-T-G

157165962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80753958-T-A

157166231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80753753-A-G

157166306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80753698-G-A

157166332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80753672-T-C

157170131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80752845-A-G

157170172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80752803-T-C

http://identifiers.org/hco/4/GRCh38#157170384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80752616-C-A

157170384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80752616-C-T

157170405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron variant
orthologous variants: 80752589-T-C

http://identifiers.org/hco/4/GRCh38#157170427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80752567-C-A

157170427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 80752567-C-T

157170818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80752180-T-C

http://identifiers.org/hco/4/GRCh38#157170912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80752085-C-A

157171209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751781-T-A

157171627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751361-G-T

157171706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751283-T-G

http://identifiers.org/hco/4/GRCh38#157171731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80751257-A-C

157171821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751178-T-C

http://identifiers.org/hco/4/GRCh38#157171869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80751132-A-C

157171885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751116-C-G

157171899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751102-A-G

157171977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: 80751025-T-C

http://identifiers.org/hco/4/GRCh38#157172014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4329
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#80750991-C-A