66813062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895428-G-A

66813062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895428-G-T

66813098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895464-A-G

66813241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895600-T-C

66813279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895640-A-G

66813309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895669-A-T

66813318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895686-T-C

66813320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895688-G-A

66813320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895688-G-T

http://identifiers.org/hco/1/GRCh38#66813332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102895700-C-A

http://identifiers.org/hco/1/GRCh38#66813334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102895707-C-A

66813476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895853-G-A

66813476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102895853-G-T

66813860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896234-T-A

66813861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896235-A-T

66813868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896242-T-C

66813888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896262-G-A

66813888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896262-G-C

66813888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896262-G-T

66813892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896270-G-A

66813898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896276-A-G

66814117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 102896475-T-G

http://identifiers.org/hco/1/GRCh38#66814213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102896574-A-C

http://identifiers.org/hco/1/GRCh38#66814282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102896652-A-C

66814282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896652-A-G

66814282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896652-A-T

66814289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896659-A-G

66814697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896769-C-T

66814779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896854-T-G

66814891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896915-A-G

66814952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896975-A-T

66814956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102896983-G-T

66815011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102897020-A-G

66815098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102897156-T-C

66815186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102897237-A-G

http://identifiers.org/hco/1/GRCh38#66815405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102897363-C-A

66815702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102897622-C-T

66815929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102897999-A-G

66815935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102898005-G-C

66816299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102898835-C-T

http://identifiers.org/hco/1/GRCh38#66817102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102899854-C-A

66818976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102901094-C-G

66819052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102901177-T-C

66821438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102904620-A-G

66821490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102904675-G-A

http://identifiers.org/hco/1/GRCh38#66821528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102904713-A-C

66821556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102904735-A-T

66821579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102904760-T-C

66821843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102904990-C-T

66822032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905149-T-C

66822209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905255-C-T

66822220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905268-G-A

66822220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905268-G-C

66822220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905268-G-T

66822237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905285-G-C

http://identifiers.org/hco/1/GRCh38#66822365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102905411-C-A

66822365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 102905411-C-G

66822365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 102905411-C-T

66822542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905592-A-G

66822557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905607-T-C

66822557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905607-T-G

66822611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905668-G-A

66822611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905668-G-T

66822771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905818-G-A

66822833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102905884-T-A

66826720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102906492-A-T

66826727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102906496-C-G

66826768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102906536-C-T

http://identifiers.org/hco/1/GRCh38#66826788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102906556-C-A

66827044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 102906820-A-G

66827096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102906874-T-C

http://identifiers.org/hco/1/GRCh38#66827200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102906984-A-C

66827296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102907074-G-A

66827697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102907189-G-T

http://identifiers.org/hco/1/GRCh38#66827730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102907218-C-A

66827730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102907218-C-T

http://identifiers.org/hco/1/GRCh38#66827796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102907280-C-A

66827796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102907280-C-T

66827902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102907386-A-G

66827967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 102907423-A-T

66830975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102913171-A-T

66831002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102913215-G-A

66831123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102913351-C-T

66831802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102914123-C-T

66831978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102914269-G-T

66832999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-G

66833020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-C

66833075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-G

66833452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102916677-C-T

66833491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102916710-A-T

http://identifiers.org/hco/1/GRCh38#66833525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102916750-A-C

66833525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102916750-A-G

66833565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102916790-A-G

66833718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102916948-G-T

66834018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 102917102-C-T

66834102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 102917186-T-A

66834102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 102917186-T-C

http://identifiers.org/hco/1/GRCh38#66834156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102917240-A-C

66834156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 102917240-A-G

66834569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102918616-T-C

http://identifiers.org/hco/1/GRCh38#66834775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102918777-C-A

66835604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919471-T-C

66835610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919477-A-G

66835656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102919523-C-T

66835667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 102919534-G-C

66835667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 102919534-G-T

66835832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919700-G-A

66835832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919700-G-C

66835860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919730-G-T

66835861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919731-G-A

66835861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919731-G-T

66836482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102919991-T-C

66836907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102920361-C-G

66836930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102920388-T-A

http://identifiers.org/hco/1/GRCh38#66837030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102920680-A-C

66837104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102920884-G-A

66837752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102921703-T-A

66837858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102921800-T-C

http://identifiers.org/hco/1/GRCh38#66837865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102921807-A-C

66837865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102921807-A-G

http://identifiers.org/hco/1/GRCh38#66837871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102921813-A-C

66837871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102921813-A-G

66839973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102922668-T-C

66840122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102922812-T-C

66840153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102922833-A-T

66840179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102922869-T-A

66840345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923010-C-T

66840363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923030-T-A

66840363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923030-T-G

66840592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 102923604-C-T

66840683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923695-A-T

66840794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923801-T-A

66840794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923801-T-C

66840795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923802-G-A

66840795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923802-G-T

http://identifiers.org/hco/1/GRCh38#66840823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102923829-C-A

66840823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923829-C-T

66840962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102923935-C-T

66845472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102927917-C-T

66846162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102928711-G-A

66846162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102928711-G-C

66846469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102928982-G-T

66846913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102929438-T-A

66846921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102929446-G-A

66846961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102929488-G-C

66847040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102929564-A-T

66847064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102929596-G-T

66847216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102929754-T-C

66847706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102930067-T-C

66847706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102930067-T-G

http://identifiers.org/hco/1/GRCh38#66847761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102930129-A-C

66847761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102930129-A-G

http://identifiers.org/hco/1/GRCh38#66847806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102930165-C-A

66847806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102930165-C-T

66861927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102939109-A-T

66862171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 102939416-A-G

66862230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102939469-T-C

66862297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 102939533-T-C

http://identifiers.org/hco/1/GRCh38#66862378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102939607-C-A

66862665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102939687-A-G

66862979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102939976-A-G

66863119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940060-G-C

66863168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940111-A-G

66863183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940122-C-T

66863290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940250-T-G

66863337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940296-A-G

66863809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940570-G-T

66863831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102940578-A-T

66870817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102943974-C-T

http://identifiers.org/hco/1/GRCh38#66870839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102943997-C-A

66870871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944029-T-A

66870871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944029-T-C

66870964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944122-G-A

66870997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944155-C-T

66871015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944173-T-C

66871037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944192-T-C

66871077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944230-T-C

66871087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944240-A-G

66871089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944242-A-G

66871125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944277-T-C

66871144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944293-A-T

66871173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944322-T-G

66871315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944475-T-C

66871330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 102944490-T-C

66871357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102944517-T-C

66871452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 102944612-A-G

66871452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 102944612-A-T

http://identifiers.org/hco/1/GRCh38#66871554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102944708-C-A

66871554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102944708-C-T

http://identifiers.org/hco/1/GRCh38#66871602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102944753-C-A

66871632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102944782-G-A

66871632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102944782-G-C

66874621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102947502-A-G

66874711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102947548-A-G

66874726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102947560-C-G

66874988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102947795-T-G

66874989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102947796-G-T

66875083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102947846-A-G

66875550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102948107-T-C

66875561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102948118-T-G

66875634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102948269-T-C

66876060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102948823-T-C

66876191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102948926-T-C

66876370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949068-T-C

66876641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949271-C-T

66876719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949343-C-G

66876776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949389-T-A

http://identifiers.org/hco/1/GRCh38#66876871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102949471-C-A

66876890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949490-C-G

66876890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949490-C-T

66876895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949495-T-G

66876939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949540-G-A

66876946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949544-A-T

66877138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949715-T-C

66877389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102949946-T-A

66877594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102950123-A-G

66891354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102952722-A-G

66891414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102952781-G-A

66891414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102952781-G-C

66891414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102952781-G-T

http://identifiers.org/hco/1/GRCh38#66893133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102953699-C-A

66893154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102953724-G-A

66893154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102953724-G-T

66893156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102953726-T-C

http://identifiers.org/hco/1/GRCh38#66893178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102953754-A-C

66893178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102953754-A-G

66893297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 102953856-T-G

66893306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 102953865-T-G

66893404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102953963-T-C

66893464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102954026-T-A

66893464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102954026-T-G

66893559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102954113-T-A

66893559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102954113-T-G

66905215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102960438-T-C

66905222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 102960448-A-G

66905254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102960480-G-T

66905262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102960488-A-G

66905296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 102960522-C-T

66905452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 102960671-T-C

66922731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102970093-C-T

66922844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102970188-T-A

66922908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102970255-T-C

http://identifiers.org/hco/1/GRCh38#66922943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#102970301-C-A

66922943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102970301-C-T

66924515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102971185-A-G

66924528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102971198-G-A

66924632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26252
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 102971277-T-C