38290959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302343-G-T

38291072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302450-T-C

38291072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302450-T-G

http://identifiers.org/hco/22/GRCh38#38291289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79302658-C-A

38291289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302658-C-T

38291336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302790-A-G

38291336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302790-A-T

38291434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302909-G-A

38291434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302909-G-T

38291454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79302929-A-G

38291534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303001-G-A

38291583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303039-G-A

38291583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303039-G-T

http://identifiers.org/hco/22/GRCh38#38291615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79303059-C-A

38291615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303059-C-T

38291643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303071-G-A

38291643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303071-G-T

38291665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303093-G-A

38291665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303093-G-T

38291712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303120-G-A

38291712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303120-G-T

38291756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303163-G-A

38291756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303163-G-T

38291921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303370-G-A

38291921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3 prime UTR variant
orthologous variants: 79303370-G-T

http://identifiers.org/hco/22/GRCh38#38291971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79303418-A-C

38291971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79303418-A-G

38291971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79303418-A-T

http://identifiers.org/hco/22/GRCh38#38291983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79303430-C-A

38291983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79303430-C-T

http://identifiers.org/hco/22/GRCh38#38292557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79303542-C-A

38292557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79303542-C-G

38292621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79303603-G-T

38292624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79303606-A-G

38292624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79303606-A-T

38292756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79303729-G-A

38292756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79303729-G-T

38292894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79303844-A-T

38292924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79303870-T-A

38292924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79303870-T-C

38292924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79303870-T-G

38293015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79303932-G-A

38293015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79303932-G-T

38293026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79303941-A-G

38293097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79304011-T-G

http://identifiers.org/hco/22/GRCh38#38293134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304044-C-A

http://identifiers.org/hco/22/GRCh38#38293159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304058-C-A

38293159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79304058-C-T

http://identifiers.org/hco/22/GRCh38#38293162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304061-C-A

38293162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79304061-C-T

http://identifiers.org/hco/22/GRCh38#38293164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304063-C-A

38293164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 79304063-C-G

38293256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 79304106-T-G

38293277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 79304126-G-C

38293383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79304212-G-T

38293621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79304431-G-A

http://identifiers.org/hco/22/GRCh38#38293659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304462-C-A

http://identifiers.org/hco/22/GRCh38#38293737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304528-C-A

38293776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79304567-T-C

http://identifiers.org/hco/22/GRCh38#38294049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304727-C-A

38294075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79304751-G-T

38294218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79304893-A-T

38294251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79304926-G-A

http://identifiers.org/hco/22/GRCh38#38294318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79304993-C-A

38294318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79304993-C-T

38294616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305292-G-A

38294616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305292-G-T

http://identifiers.org/hco/22/GRCh38#38294655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79305328-C-A

38294691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305368-C-T

http://identifiers.org/hco/22/GRCh38#38294811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79305455-A-C

38294850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305494-C-G

38295075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305647-C-T

38295226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305762-C-T

38295271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305801-G-C

38295271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305801-G-T

38295309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305839-A-G

38295309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305839-A-T

http://identifiers.org/hco/22/GRCh38#38295346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79305876-C-A

38295346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79305876-C-T

38295529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306057-A-G

38295565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306083-T-C

http://identifiers.org/hco/22/GRCh38#38295575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79306093-C-A

38295575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306093-C-T

http://identifiers.org/hco/22/GRCh38#38296076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79306576-C-A

38296076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306576-C-T

38296085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306585-G-A

38296085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306585-G-C

38296085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306585-G-T

38296097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306597-T-A

38296097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306597-T-C

http://identifiers.org/hco/22/GRCh38#38296133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79306620-A-C

38296133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306620-A-G

38296195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79306670-C-T

38296205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79306680-G-A

38296205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79306680-G-T

38296240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79306716-T-A

38296240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79306716-T-C

38296240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79306716-T-G

http://identifiers.org/hco/22/GRCh38#38296388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79306854-C-A

38296439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79306929-T-C

http://identifiers.org/hco/22/GRCh38#38296535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79307033-C-A

38296535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 79307033-C-T

38296570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 79307061-G-A

38296570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 79307061-G-T

38296586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 79307077-G-A

38296665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 79307146-T-C

38296672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79307158-A-T

38296721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307202-C-T

38296722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307203-T-C

38296723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307204-T-C

38296738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307221-G-A

38296739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307222-G-T

38297043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307396-G-A

38297043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307396-G-T

38297061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307413-A-G

http://identifiers.org/hco/22/GRCh38#38297166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79307430-C-A

38297300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307563-A-G

http://identifiers.org/hco/22/GRCh38#38297305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79307568-C-A

http://identifiers.org/hco/22/GRCh38#38297323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79307588-C-A

38297627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307869-G-C

38297627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307869-G-T

38297649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307891-G-A

38297706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307945-G-A

38297706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307945-G-T

38297712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307947-T-C

38297736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307972-G-A

38297736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307972-G-T

http://identifiers.org/hco/22/GRCh38#38297738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79307974-C-A

38297738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79307974-C-T

38297763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308017-G-A

38297763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308017-G-T

http://identifiers.org/hco/22/GRCh38#38297774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79308026-A-C

38297774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308026-A-G

38297791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308045-G-A

38297805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308059-G-T

38297806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308060-G-A

38297806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308060-G-C

38297818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308072-A-G

38297941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79308195-C-T

38297948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79308202-T-C

38298096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: 79308354-G-T

38298247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308499-T-C

38298247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 79308499-T-G

http://identifiers.org/hco/22/GRCh38#38298339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79308593-C-A

38298400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79308654-C-T

http://identifiers.org/hco/22/GRCh38#38298577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79308825-C-A

38298577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 79308825-C-G

38298582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 79308830-T-C

38298597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 79308845-A-G

38298955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79309206-T-C

38298964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79309215-C-T

38299009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79309261-C-T

38299383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79309528-T-C

38299826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79309651-G-T

38299880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79309685-C-T

38299944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 79309749-G-A

38300136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79309908-T-C

38300148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79309920-T-C

38300201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79309969-A-G

38300201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79309969-A-T

38300235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310004-A-G

38300352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310118-G-A

38300511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310259-G-A

38300511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310259-G-C

38300512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310260-C-T

38300583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310321-T-C

38300583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310321-T-G

38300658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310406-G-A

38300658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310406-G-C

38300658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310406-G-T

38300767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: 79310502-G-A

38300767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: 79310502-G-C

38300967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310702-G-A

38300967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79310702-G-T

38302825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79313824-G-A

38302832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79313831-G-C

38302870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: 79313921-G-A

http://identifiers.org/hco/22/GRCh38#38302885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79313936-C-A

38302885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: 79313936-C-G

38302885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: 79313936-C-T

38303017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79314066-T-G

38303033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314082-T-C

38303047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314103-G-C

38303097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314209-G-A

38303097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314209-G-C

38303097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314209-G-T

38303111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314223-G-A

38303111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314223-G-C

38303111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314223-G-T

38303118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314230-G-A

38303118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314230-G-C

38303118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314230-G-T

http://identifiers.org/hco/22/GRCh38#38303125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79314243-A-C

38303157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: synonymous variant
orthologous variants: 79314274-G-A

38303157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: stop gained
orthologous variants: 79314274-G-T

http://identifiers.org/hco/22/GRCh38#38303252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79314369-C-A

38303252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 79314369-C-T

http://identifiers.org/hco/22/GRCh38#38303294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79314409-C-A

38303294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314409-C-T

38303297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314412-G-A

38303297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314412-G-T

http://identifiers.org/hco/22/GRCh38#38303304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79314419-C-A

38303304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314419-C-T

38303334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314449-G-A

38303334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314449-G-T

38303338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314453-T-C

38303377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314491-G-A

38303377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314491-G-C

38303377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314491-G-T

38303394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314508-G-A

38303394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314508-G-T

http://identifiers.org/hco/22/GRCh38#38303399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79314513-A-C

38303399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79314513-A-G

38308139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79317679-C-T

38309904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79319663-C-G

38309924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79319676-C-T

38310101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79319850-G-A

38310101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79319850-G-C

38310195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320025-G-A

38310259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320088-T-A

38310381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320217-G-A

38310913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320790-C-G

38311212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320877-C-T

38311213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320878-G-A

38311353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79320990-T-C

38311461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, undefined
orthologous variants: 79321098-G-C

38312539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79321441-C-T

38313048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322031-T-C

38313076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322059-C-T

38313319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322307-C-G

38313413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron_variant, undefined
orthologous variants: 79322396-T-C

38313951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322840-G-A

38313951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322840-G-T

38313983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322882-G-T

38314017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322908-G-T

38314045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79322935-G-T

38314151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: missense variant
orthologous variants: 79323041-G-T

38314243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79323138-G-A

38314243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79323138-G-T

38314889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79323992-C-T

38314954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79324055-A-G

38315177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79324313-C-T

http://identifiers.org/hco/22/GRCh38#38316061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79325210-A-C

38316219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79325395-T-C

38316537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79325669-G-C

38316537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79325669-G-T

38316579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79325711-T-C

38316790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79325882-G-A

38316790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79325882-G-C

http://identifiers.org/hco/22/GRCh38#38316853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79325942-C-A

http://identifiers.org/hco/22/GRCh38#38317075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#79326070-C-A

38317075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79326070-C-T

38317264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79326184-G-A

38317264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 79326184-G-T

38317808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79326503-T-C

38317865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2453
most severe consequence: intron variant
orthologous variants: 79326552-A-G