960595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319289-A-G

960595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319289-A-T

http://identifiers.org/hco/1/GRCh38#960596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319285-C-A

960596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319285-C-G

960596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319285-C-T

960600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319281-G-A

960600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319281-G-T

960623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319260-G-A

960623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319260-G-C

960623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319260-G-T

http://identifiers.org/hco/1/GRCh38#960626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319257-C-A

960626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319257-C-G

960626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319257-C-T

http://identifiers.org/hco/1/GRCh38#960670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319227-A-C

960670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319227-A-G

960670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5 prime UTR variant
orthologous variants: 156319227-A-T

http://identifiers.org/hco/1/GRCh38#960715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319190-C-A

960715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156319190-C-G

960715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156319190-C-T

http://identifiers.org/hco/1/GRCh38#960730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319175-C-A

960730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156319175-C-G

960730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: stop gained
orthologous variants: 156319175-C-T

http://identifiers.org/hco/1/GRCh38#960785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319126-C-A

960785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156319126-C-G

960785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156319126-C-T

http://identifiers.org/hco/1/GRCh38#960790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319121-C-A

960790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156319121-C-G

960808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 156319103-G-A

960812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156319099-G-A

960812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156319099-G-C

960812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156319099-G-T

http://identifiers.org/hco/1/GRCh38#960822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156319087-C-A

960822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156319087-C-G

960822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156319087-C-T

http://identifiers.org/hco/1/GRCh38#960858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318945-C-A

960858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318945-C-T

960884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318920-G-A

960884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318920-G-T

http://identifiers.org/hco/1/GRCh38#960894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318910-C-A

960906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318899-G-A

960906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318899-G-C

960906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318899-G-T

960921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318865-G-A

960921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318865-G-T

960980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318812-G-A

960984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318808-C-T

961005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318791-G-A

961005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318791-G-T

961055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318758-G-A

961059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318754-G-A

961059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318754-G-T

961070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318737-T-C

961095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156318713-C-T

961147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318661-G-T

http://identifiers.org/hco/1/GRCh38#961151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318657-C-A

961151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318657-C-G

961151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318657-C-T

961152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318656-T-C

961152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318656-T-G

http://identifiers.org/hco/1/GRCh38#961167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318638-C-A

961167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318638-C-G

961167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318638-C-T

http://identifiers.org/hco/1/GRCh38#961182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318623-C-A

961182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318623-C-T

961198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318617-G-A

961205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318610-T-C

961253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318562-G-A

http://identifiers.org/hco/1/GRCh38#961257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318557-C-A

961257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318557-C-G

961261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318553-G-A

961261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318553-G-C

961261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318553-G-T

http://identifiers.org/hco/1/GRCh38#961275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318537-C-A

961275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318537-C-G

961275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318537-C-T

http://identifiers.org/hco/1/GRCh38#961283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318527-C-A

961283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 156318527-C-T

961316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156318494-C-G

961316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156318494-C-T

961322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156318488-A-G

http://identifiers.org/hco/1/GRCh38#961334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318476-C-A

961334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 156318476-C-T

961357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156318453-C-G

961357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: stop gained
orthologous variants: 156318453-C-T

961426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156318384-G-A

961426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156318384-G-T

961489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156318321-G-A

http://identifiers.org/hco/1/GRCh38#961495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156318315-C-A

961495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156318315-C-T

961537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156318273-C-T

961561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156318240-C-G

961561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156318240-C-T

961604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156318193-C-T

961617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156318180-C-T

961688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156318109-T-C

961724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156318073-A-G

961773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156318026-C-T

961775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156318024-C-T

961802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 156317974-C-T

962003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156317723-G-A

http://identifiers.org/hco/1/GRCh38#962090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156317609-A-C

962090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317609-A-G

962090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317609-A-T

http://identifiers.org/hco/1/GRCh38#962120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156317520-C-A

962120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317520-C-G

962120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317520-C-T

http://identifiers.org/hco/1/GRCh38#962145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156317468-C-A

962145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317468-C-G

962145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317468-C-T

962274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156317282-C-T

962297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156317255-G-A

962297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 156317255-G-T

http://identifiers.org/hco/1/GRCh38#962298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156317254-C-A

962298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156317254-C-G

962298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156317254-C-T

962320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156317236-C-T

962442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156317113-G-A

962442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 156317113-G-C

http://identifiers.org/hco/1/GRCh38#962507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156317051-A-C

962507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156317051-A-G

http://identifiers.org/hco/1/GRCh38#962525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156317033-C-A

962525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156317033-C-T

http://identifiers.org/hco/1/GRCh38#962551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316998-C-A

962551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316998-C-T

962577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316972-T-C

962580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316969-T-C

962601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316951-G-A

962601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316951-G-T

http://identifiers.org/hco/1/GRCh38#962609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316943-C-A

962613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316939-C-T

962622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316930-C-T

962641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316913-C-T

http://identifiers.org/hco/1/GRCh38#962664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316891-C-A

962664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316891-C-G

962664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316891-C-T

962666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316890-G-A

962666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316890-G-C

962666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316890-G-T

http://identifiers.org/hco/1/GRCh38#962673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316883-C-A

962673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316883-C-T

962679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316877-G-T

http://identifiers.org/hco/1/GRCh38#962681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316875-C-A

962681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316875-C-T

962686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316871-G-A

962686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156316871-G-T

962716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156316843-G-A

962716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156316843-G-T

962764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316795-G-A

962764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316795-G-T

962800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316759-G-A

962800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316759-G-T

http://identifiers.org/hco/1/GRCh38#962860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316699-A-C

962860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316699-A-G

962890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316669-G-A

962890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316669-G-T

http://identifiers.org/hco/1/GRCh38#962899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316660-C-A

962899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316660-C-T

962914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316645-G-T

962919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 156316640-T-C

962919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, splice_donor_variant
orthologous variants: 156316640-T-G

962935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156316621-T-C

962956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156316600-T-G

962970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156316584-G-A

962970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156316584-G-T

http://identifiers.org/hco/1/GRCh38#962997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316546-C-A

http://identifiers.org/hco/1/GRCh38#963022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316502-C-A

963022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156316502-C-T

963069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 156316463-G-A

http://identifiers.org/hco/1/GRCh38#963085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156316448-C-A

963085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 156316448-C-T

963102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 156316408-T-G

963146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 156316364-G-A

963216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 156316294-G-A

963216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 156316294-G-T

963222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 156316288-G-A

963222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 156316288-G-C

963222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 156316288-G-T

963310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 156316195-T-C

963314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156316191-C-G

963314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 156316191-C-T

963539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315964-G-C

963552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315947-A-G

963605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315888-G-A

963605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315888-G-T

963624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315864-T-C

963624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315864-T-G

http://identifiers.org/hco/1/GRCh38#963642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315845-A-C

963642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315845-A-G

963759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315786-A-G

http://identifiers.org/hco/1/GRCh38#963764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315781-C-A

963764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315781-C-G

963764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315781-C-T

http://identifiers.org/hco/1/GRCh38#963771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315774-C-A

963771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315774-C-T

http://identifiers.org/hco/1/GRCh38#963782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315762-C-A

963782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315762-C-T

963819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315731-C-G

963819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 156315731-C-T

http://identifiers.org/hco/1/GRCh38#963942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315606-A-C

964035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156315503-C-G

964035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 156315503-C-T

964212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315323-C-T

964244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315281-T-C

964244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315281-T-G

http://identifiers.org/hco/1/GRCh38#964253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315272-C-A

964253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315272-C-T

964256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315248-C-T

964304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315188-G-A

964304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315188-G-T

964321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315171-T-C

http://identifiers.org/hco/1/GRCh38#964336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156315156-C-A

964336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315156-C-T

964338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315154-C-G

964338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 156315154-C-T

964355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 156315135-G-A

964367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 156315123-G-A

964448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 156315042-G-A

964448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 156315042-G-T

964451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 156315039-A-G

964548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314944-G-A

964548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314944-G-C

964548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314944-G-T

964562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314930-G-A

964562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314930-G-C

964562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314930-G-T

http://identifiers.org/hco/1/GRCh38#964569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314923-C-A

964569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314923-C-G

964569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314923-C-T

964954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: intron variant
orthologous variants: 156314726-T-A

964970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314710-C-T

965015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314665-A-G

965078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314602-G-A

965081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314599-G-A

965081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314599-G-C

965081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314599-G-T

965102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314578-C-T

965114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314566-G-T

965120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314560-G-A

965120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314560-G-T

965144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: missense variant
orthologous variants: 156314536-C-T

965196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314484-C-G

965217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314458-C-T

965234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314392-G-C

965241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314385-G-A

965244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314382-G-A

965244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314382-G-C

965244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314382-G-T

http://identifiers.org/hco/1/GRCh38#965258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314368-C-A

965258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314368-C-G

965258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314368-C-T

965264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314362-G-A

965264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314362-G-C

965264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314362-G-T

965270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314357-T-C

965270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314357-T-G

http://identifiers.org/hco/1/GRCh38#965298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314329-C-A

965298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314329-C-T

http://identifiers.org/hco/1/GRCh38#965319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314303-A-C

965319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314303-A-G

965319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314303-A-T

965327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314295-A-G

965327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314295-A-T

965356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314260-G-A

965356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314260-G-T

http://identifiers.org/hco/1/GRCh38#965364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314252-A-C

965364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314252-A-G

965364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314252-A-T

965370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314246-G-A

965370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314246-G-C

965370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314246-G-T

965416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314167-C-T

965424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314159-T-A

965424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314159-T-C

965424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314159-T-G

965430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314153-G-A

965430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314153-G-T

965439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314144-G-A

965439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314144-G-T

965472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314113-G-A

965472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314113-G-T

http://identifiers.org/hco/1/GRCh38#965474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314110-C-A

http://identifiers.org/hco/1/GRCh38#965495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314089-C-A

965495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314089-C-T

965496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314088-A-G

965500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314084-T-C

965503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314065-G-A

965503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314065-G-T

965517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314051-T-C

http://identifiers.org/hco/1/GRCh38#965543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314016-C-A

965543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314016-C-G

965543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314016-C-T

http://identifiers.org/hco/1/GRCh38#965549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#156314009-C-A

965549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156314009-C-T

965610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156313925-T-C

965610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24023
most severe consequence: 3 prime UTR variant
orthologous variants: 156313925-T-G