108986413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41784443-T-A

108986713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41784144-T-C

108987282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783617-G-C

108987282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783617-G-T

108987324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783572-A-G

108987340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783556-A-T

http://identifiers.org/hco/6/GRCh38#108987361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41783535-C-A

108987361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783535-C-T

108987391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783506-T-G

108987440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783458-T-C

108987671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41783225-G-A

108987671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41783225-G-T

http://identifiers.org/hco/6/GRCh38#108988350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41782617-C-A

108988356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41782611-T-G

http://identifiers.org/hco/6/GRCh38#108988413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41782580-A-C

108988413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782580-A-G

108988428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782565-T-C

108988448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782545-G-A

108988448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782545-G-C

108988448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782545-G-T

108988460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782535-G-A

108988460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782535-G-T

108988503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41782508-T-C

108988697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41782320-G-A

108988698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41782319-A-G

108988795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41782253-G-A

108988908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41782152-C-T

108988913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41782147-G-A

108988913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41782147-G-C

108988919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41782141-C-T

108990513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41781471-G-A

108990513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41781471-G-T

http://identifiers.org/hco/6/GRCh38#108990514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41781470-C-A

108990514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41781470-C-G

http://identifiers.org/hco/6/GRCh38#108990563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41781442-C-A

108990606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41781396-A-G

108990753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41781250-T-C

108990903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41781099-T-C

http://identifiers.org/hco/6/GRCh38#108990947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41781076-C-A

108990947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41781076-C-T

108991182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780915-T-C

108991692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780628-A-G

108991693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780627-A-G

108991803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780519-T-C

108991931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780415-T-G

108991938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780409-T-C

108992305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780155-A-T

108992457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41780109-C-G

108992726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779857-G-A

108992726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41779857-G-T

108992937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41779641-G-A

108992937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41779641-G-T

http://identifiers.org/hco/6/GRCh38#108992961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41779624-C-A

108992961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41779624-C-T

108994313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778819-A-T

108994341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778794-T-C

108994360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778774-G-C

108994360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778774-G-T

108994375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778761-G-C

108994375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778761-G-T

108994402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778734-T-A

108994666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778467-A-G

108994666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778467-A-T

108995275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778190-T-A

108995275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778190-T-C

108995386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778111-A-G

108995426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41778073-C-T

108995930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777599-T-C

108995990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777547-C-T

108996043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777519-G-A

108996043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777519-G-T

108996099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777467-G-A

108996222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777390-A-G

108996278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777346-G-A

108996306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777319-T-G

http://identifiers.org/hco/6/GRCh38#108996414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41777219-A-C

108996420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777174-T-C

108996420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41777174-T-G

108997068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41776537-T-C

108997514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41776110-A-G

108998547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41774385-T-G

108998718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41774214-G-A

108998718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41774214-G-C

108998760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41774172-G-A

108998760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41774172-G-T

108998761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41774171-G-A

108998761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41774171-G-T

108998770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41774162-A-G

108998990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41773952-T-C

108999021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41773919-T-C

108999100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41773855-T-A

108999125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41773832-A-G

108999518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41773429-G-T

http://identifiers.org/hco/6/GRCh38#108999732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41773265-C-A

108999732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41773265-C-T

108999845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41773187-C-T

http://identifiers.org/hco/6/GRCh38#108999870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41773162-C-A

108999870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41773162-C-T

http://identifiers.org/hco/6/GRCh38#109000431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41772257-C-A

109000431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41772257-C-G

109000472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41772205-A-G

109000519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41772171-G-A

109000519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41772171-G-T

109000721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41771965-T-C

109000754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41771937-G-A

109000754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41771937-G-T

http://identifiers.org/hco/6/GRCh38#109000780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41771917-C-A

109000809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41771890-T-G

http://identifiers.org/hco/6/GRCh38#109000821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41771878-C-A

109001564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41770742-C-T

109001621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41770695-T-C

109002009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41770365-T-C

http://identifiers.org/hco/6/GRCh38#109002154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41770221-A-C

109002154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41770221-A-G

109002154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41770221-A-T

109002217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41770161-G-T

109002312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 41770067-C-T

109002863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41769544-A-T

109003085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41769400-A-G

109003899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41767942-C-G

109004199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41767692-A-G

109006147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41766223-G-A

109006974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41765987-T-C

109007610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41765182-T-C

109007690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41765098-T-G

109008077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41764711-C-G

http://identifiers.org/hco/6/GRCh38#109008429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41764332-A-C

109008735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41764040-G-A

109008735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41764040-G-T

109008763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41764020-A-T

109008777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41764002-G-T

http://identifiers.org/hco/6/GRCh38#109008857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763941-C-A

109008857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763941-C-T

109008858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763940-T-C

109008861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763937-T-C

109008864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763934-C-T

109008875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763928-G-A

109008875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763928-G-T

109008904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763879-T-C

109008904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41763879-T-G

109009057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763739-G-A

109009057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763739-G-C

109009057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763739-G-T

http://identifiers.org/hco/6/GRCh38#109009077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763720-C-A

109009236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763662-T-G

109009329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763618-A-T

http://identifiers.org/hco/6/GRCh38#109009338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763612-C-A

109009338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763612-C-G

109009338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763612-C-T

109009371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41763577-G-A

109009371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 41763577-G-T

http://identifiers.org/hco/6/GRCh38#109009375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763573-C-A

109009375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant
orthologous variants: 41763573-C-T

109009429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant
orthologous variants: 41763519-T-C

http://identifiers.org/hco/6/GRCh38#109009452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763496-C-A

109009452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 41763496-C-G

109009452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 41763496-C-T

109009457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 41763491-G-A

109009457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 41763491-G-C

109009457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 41763491-G-T

http://identifiers.org/hco/6/GRCh38#109009518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763465-C-A

109009518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41763465-C-G

109009518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41763465-C-T

http://identifiers.org/hco/6/GRCh38#109009521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763462-C-A

109009521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41763462-C-G

109009521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41763462-C-T

109009569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: 41763414-G-A

http://identifiers.org/hco/6/GRCh38#109009668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41763316-C-A

109009668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41763316-C-T

http://identifiers.org/hco/6/GRCh38#109011232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41761717-C-A

109012094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41760406-C-T

109012736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41759902-G-A

109013633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41759223-A-T

109013691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41759174-A-T

109014029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41758860-A-T

109014202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41758684-C-T

109014277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41758604-T-C

109014345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41758537-T-C

109014345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41758537-T-G

109015720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41757365-G-A

http://identifiers.org/hco/6/GRCh38#109020869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41756168-A-C

109022083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41755253-A-T

109022192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41754906-G-A

109029039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41749792-C-G

109029151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41749718-G-C

109029272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41749602-T-C

109029902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748983-T-C

109030238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748638-G-C

109030258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748619-T-A

109030258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748619-T-G

109030364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748521-A-G

109030441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748453-G-C

109030441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748453-G-T

109030586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748351-T-C

http://identifiers.org/hco/6/GRCh38#109030633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41748307-C-A

109030749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748206-A-G

109030828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41748129-T-A

109033279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747596-G-A

http://identifiers.org/hco/6/GRCh38#109033307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41747568-C-A

109033525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747383-T-C

109033684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747226-G-A

http://identifiers.org/hco/6/GRCh38#109033791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41747115-A-C

109033796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747106-T-C

109033796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747106-T-G

109033869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747038-T-C

109033880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41747027-C-G

109033943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41746947-G-A

109037484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41741598-C-T

109037574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41741508-G-C

109038647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41740086-G-A

109038705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41740043-G-T

109039229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41739885-G-A

109039393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41739761-A-G

109039736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41739411-A-G

109040304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41739009-C-T

109040387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41738945-G-C

109040387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41738945-G-T

109040494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41738841-G-A

109040589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41738757-G-A

109040934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41738458-G-A

109052686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41729589-G-A

109053109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41728938-T-C

109053271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41728777-A-G

http://identifiers.org/hco/6/GRCh38#109053546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41728573-A-C

109055381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41726628-G-T

109055740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41726608-G-C

109055745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41726603-C-T

109056757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41725414-T-C

109057072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41725170-T-C

109057476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41724872-T-G

http://identifiers.org/hco/6/GRCh38#109057620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41724726-C-A

109057707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41724651-C-T

109058611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41724183-C-T

109058690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41724106-A-G

109058697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41724099-C-T

http://identifiers.org/hco/6/GRCh38#109058752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41724044-A-C

109058752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41724044-A-G

http://identifiers.org/hco/6/GRCh38#109058841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41723883-C-A

109058894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41723831-C-T

109059207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41716442-G-C

109059207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41716442-G-T

109059221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41716425-T-C

109059848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41715221-C-T

109059849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41715220-G-A

109059966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41715097-C-T

109060492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41714746-G-C

109060612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41714640-C-T

109060814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41714468-C-G

109060814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41714468-C-T

109063784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41714150-C-T

http://identifiers.org/hco/6/GRCh38#109065137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41712396-C-A

109065240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41712304-T-C

109065594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41712004-A-G

109065623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41711975-T-C

109065751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41711813-T-C

109066003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41711608-G-A

109066003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41711608-G-C

109066362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41711257-G-A

109066791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41710743-C-T

109066927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41710609-G-A

109066929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41710607-A-G

109070385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41710101-C-T

109070715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41709781-T-C

109070808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41709570-G-T

109071249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41709175-C-T

109071956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41707915-C-T

109072123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41707760-T-A

http://identifiers.org/hco/6/GRCh38#109073485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41707139-C-A

109074469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41705715-A-G

109074938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704928-G-A

109074938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704928-G-T

109075026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704839-C-T

109075074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704793-T-C

http://identifiers.org/hco/6/GRCh38#109075181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41704696-C-A

109075181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704696-C-T

109075430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704442-C-T

109075586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704323-A-G

http://identifiers.org/hco/6/GRCh38#109075683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41704221-C-A

109075683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704221-C-T

109075705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41704199-G-C

109076067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41703868-T-A

109076433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41703525-T-G

109076554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41703179-T-C

109076757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41703002-T-G

109076947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41702849-A-G

109079081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41700639-G-A

109079443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699887-T-C

109079783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699213-T-C

109079870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699131-G-A

109079921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699078-C-G

109079927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699072-T-A

109079995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699004-T-A

109079995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41699004-T-C

109080139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41698860-A-T

109082171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41697632-T-A

109082289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41697501-C-T

109082608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41697262-C-T

109082649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41697221-C-G

109082729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41697136-G-T

109082957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41696928-G-A

109083877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41695469-A-T

109084058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41695291-C-T

109084251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41695096-T-G

109084953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41693818-G-A

109085028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41693746-A-T

http://identifiers.org/hco/6/GRCh38#109085142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41693645-C-A

http://identifiers.org/hco/6/GRCh38#109085637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41693503-A-C

109086691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41693102-G-T

109087416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41692288-G-T

109087498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41692218-G-A

109087987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41691608-G-T

109087988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41691607-G-A

109087988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41691607-G-T

http://identifiers.org/hco/6/GRCh38#109088006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41691589-C-A

109088006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: 41691589-C-T

http://identifiers.org/hco/6/GRCh38#109088015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41691580-A-C

http://identifiers.org/hco/6/GRCh38#109088146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41691486-C-A

109088146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41691486-C-G

109088146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41691486-C-T

109088184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 41691457-C-T

109088736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41691065-G-A

http://identifiers.org/hco/6/GRCh38#109089616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41690283-A-C

109089634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41690265-T-C

109089738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41690205-C-T

http://identifiers.org/hco/6/GRCh38#109089968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41690009-C-A

109090013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41689966-G-A

109090072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41689920-G-C

109091440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41689702-C-G

109091712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41689369-G-T

109092471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41688651-C-T

109093298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41687813-G-A

109093608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41687539-G-A

http://identifiers.org/hco/6/GRCh38#109093765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41687314-C-A

109093918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41687171-C-T

http://identifiers.org/hco/6/GRCh38#109094154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41686904-A-C

109094187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41686870-A-G

109094276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: 41686767-A-G

http://identifiers.org/hco/6/GRCh38#109094389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41686653-C-A

http://identifiers.org/hco/6/GRCh38#109094510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41686537-C-A

109094510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: 41686537-C-T

109094585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: 41686458-C-T

109094598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: 41686445-G-A

109094695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41686358-G-A

http://identifiers.org/hco/6/GRCh38#109094802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41686250-A-C

109094802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 41686250-A-G

109094821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21595
most severe consequence: 5 prime UTR variant
orthologous variants: 41686232-T-G