38530323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400457-G-A

38530323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400457-G-T

38530356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400491-G-A

38530356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400491-G-T

38530410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400547-G-A

38530410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400547-G-C

38530410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400547-G-T

http://identifiers.org/hco/17/GRCh38#38530533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97400673-C-A

38530533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400673-C-T

http://identifiers.org/hco/17/GRCh38#38530593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97400732-C-A

38530593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400732-C-T

http://identifiers.org/hco/17/GRCh38#38530619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97400760-C-A

38530652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400793-A-T

http://identifiers.org/hco/17/GRCh38#38530675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97400816-A-C

38530675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400816-A-G

38530724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97400850-A-G

http://identifiers.org/hco/17/GRCh38#38530912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97401014-C-A

38530985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97401099-A-G

38530987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97401101-G-A

38530987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97401101-G-T

38530993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97401107-G-T

38531086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97401184-T-C

38531950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402038-T-C

http://identifiers.org/hco/17/GRCh38#38531977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402069-C-A

http://identifiers.org/hco/17/GRCh38#38531984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402076-C-A

38531984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402076-C-T

http://identifiers.org/hco/17/GRCh38#38531994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402085-C-A

38531994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402085-C-T

http://identifiers.org/hco/17/GRCh38#38532017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402105-C-A

38532017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402105-C-T

http://identifiers.org/hco/17/GRCh38#38532064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402151-C-A

38532069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402156-G-A

38532069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402156-G-T

38532196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402275-T-A

38532196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402275-T-C

38532292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402358-C-T

38532293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402359-G-T

http://identifiers.org/hco/17/GRCh38#38532307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402372-C-A

38532307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402372-C-T

38532511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402565-A-G

38532511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402565-A-T

http://identifiers.org/hco/17/GRCh38#38532617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402684-C-A

38532617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402684-C-T

http://identifiers.org/hco/17/GRCh38#38532624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97402690-C-A

38532684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402744-T-G

38532960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402997-G-A

38532960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97402997-G-T

http://identifiers.org/hco/17/GRCh38#38533068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97403140-A-C

38533068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403140-A-T

38533155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403214-G-A

38533155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403214-G-C

38533155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403214-G-T

http://identifiers.org/hco/17/GRCh38#38533188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97403237-C-A

38533188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403237-C-G

38533188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403237-C-T

38533284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403327-G-C

38533284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3 prime UTR variant
orthologous variants: 97403327-G-T

38533480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97403523-C-T

http://identifiers.org/hco/17/GRCh38#38533568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97403619-A-C

38533568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97403619-A-G

38533617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97403688-G-A

38533617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97403688-G-C

38533617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97403688-G-T

http://identifiers.org/hco/17/GRCh38#38533767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97403844-A-C

38533767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97403844-A-G

38534517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97404516-A-T

38534865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97404899-C-T

38534898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97404931-C-T

38540211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97406894-G-A

38540324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97406988-T-C

38540531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407098-G-A

38540575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407115-A-G

38540584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407119-C-T

38540602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407134-C-T

38540673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407198-G-A

38540718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407233-G-A

38540849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407317-G-A

38540928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407391-A-G

38540929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407392-T-C

38540929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97407392-T-G

38542436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408427-C-T

38542438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408429-C-T

38542533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408497-G-T

38542577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408544-C-T

38542578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408545-T-C

38542578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408545-T-G

38542600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408563-G-A

38542600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408563-G-T

38542666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408620-A-G

38542667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408621-G-A

38542667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408621-G-T

http://identifiers.org/hco/17/GRCh38#38542694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97408642-C-A

38542694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408642-C-T

http://identifiers.org/hco/17/GRCh38#38542711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97408658-C-A

38542711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408658-C-T

38542719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408666-G-T

http://identifiers.org/hco/17/GRCh38#38542744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97408698-C-A

38542744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408698-C-T

http://identifiers.org/hco/17/GRCh38#38542806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97408759-C-A

38542806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408759-C-T

http://identifiers.org/hco/17/GRCh38#38542847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97408786-C-A

38542966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408857-A-T

38543021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408913-A-T

38543057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97408948-G-C

38543169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409045-G-T

38543170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409046-C-T

38543258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409091-A-G

38543267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409100-G-T

http://identifiers.org/hco/17/GRCh38#38543276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97409109-C-A

38543548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409240-G-A

38543646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409298-G-A

38543646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409298-G-C

38543904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97409517-G-T

38543918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97409531-G-A

38543918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97409531-G-T

38544011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409620-G-A

38544025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409625-A-G

38544039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409639-T-G

38544046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409646-G-A

38544046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409646-G-T

38544072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409678-G-C

38544072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409678-G-T

38544372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97409954-C-G

38544506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97410073-G-A

38544506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97410073-G-T

38544576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97410138-G-T

38544862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410423-A-G

38545102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410663-G-T

38545129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410690-G-T

http://identifiers.org/hco/17/GRCh38#38545139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97410700-C-A

38545145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410706-T-C

38545206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410746-A-G

38545220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410760-T-A

38545220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410760-T-C

38545220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410760-T-G

38545221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410761-G-A

38545221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410761-G-C

http://identifiers.org/hco/17/GRCh38#38545238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97410778-C-A

38545238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410778-C-T

38545258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97410798-C-T

http://identifiers.org/hco/17/GRCh38#38545271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97410811-C-A

38545271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410811-C-G

38545271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410811-C-T

38545402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97410942-G-A

38545402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97410942-G-T

38545431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97410971-A-G

38545439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410979-G-A

38545444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97410984-T-A

38545444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97410984-T-C

38545454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410994-G-A

38545454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97410994-G-T

http://identifiers.org/hco/17/GRCh38#38545519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97411062-A-C

38545519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411062-A-G

38545605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411148-G-A

38545605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411148-G-C

38545605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411148-G-T

http://identifiers.org/hco/17/GRCh38#38545708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97411239-C-A

38545708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411239-C-T

38545791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411304-C-T

38545816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411327-G-A

38545891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411401-G-A

38545916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411438-A-G

http://identifiers.org/hco/17/GRCh38#38545919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97411441-C-A

38545925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411447-G-A

38546007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411513-G-C

38546171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411682-T-G

http://identifiers.org/hco/17/GRCh38#38546403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97411899-C-A

38546403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411899-C-G

38546403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411899-C-T

38546431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97411929-G-A

http://identifiers.org/hco/17/GRCh38#38546661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97412138-A-C

38546661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97412138-A-G

38546670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97412146-G-T

38546735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412194-G-A

38546735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412194-G-T

http://identifiers.org/hco/17/GRCh38#38546745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97412204-C-A

38546745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412204-C-G

38546745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412204-C-T

http://identifiers.org/hco/17/GRCh38#38546779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97412235-C-A

38546779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412235-C-G

38546779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412235-C-T

http://identifiers.org/hco/17/GRCh38#38546789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97412245-C-A

38546789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412245-C-T

http://identifiers.org/hco/17/GRCh38#38546802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97412257-A-C

38546802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412257-A-G

38546802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412257-A-T

38546917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412373-C-G

38546917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412373-C-T

38546971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412425-C-G

38547062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412503-T-A

38547062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412503-T-C

38547118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412551-C-G

38547186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97412624-C-T

38547561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413009-G-A

38547631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413094-G-A

38547631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413094-G-C

38547631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413094-G-T

38547642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413096-T-C

38547642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413096-T-G

38547684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413135-G-A

38547684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413135-G-T

http://identifiers.org/hco/17/GRCh38#38547829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97413269-A-C

38547829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97413269-A-G

http://identifiers.org/hco/17/GRCh38#38547879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97413319-C-A

38547879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 97413319-C-T

38547938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413361-G-A

38547938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413361-G-T

http://identifiers.org/hco/17/GRCh38#38547946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97413369-C-A

38547951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413374-G-A

38547951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413374-G-T

http://identifiers.org/hco/17/GRCh38#38547958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97413381-C-A

38547958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413381-C-T

http://identifiers.org/hco/17/GRCh38#38548087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97413500-C-A

38548110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413521-C-T

38548177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413589-G-A

38548241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413657-G-T

38548255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413658-G-A

38548315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413741-G-A

http://identifiers.org/hco/17/GRCh38#38548378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97413799-A-C

38548389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413810-C-G

38548523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413885-T-C

38548545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97413904-G-T

38548584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97413943-G-A

38548584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97413943-G-C

38548584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97413943-G-T

38548593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97413952-G-A

38548593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97413952-G-T

38548620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97413979-T-C

38548689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97414048-C-G

38548724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414081-A-G

38548745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414102-T-C

38548751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414108-A-T

http://identifiers.org/hco/17/GRCh38#38548793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97414120-C-A

38548793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414120-C-T

38548837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414132-G-C

38548837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414132-G-T

38548854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414154-A-G

38548854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414154-A-T

http://identifiers.org/hco/17/GRCh38#38548930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97414218-C-A

38548930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414218-C-T

38549010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414249-A-G

38549010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414249-A-T

38549043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414270-G-A

38549043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414270-G-T

38549049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97414276-G-A

38549050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414277-T-C

38549050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414277-T-G

38549107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97414334-T-A

38549107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97414334-T-G

http://identifiers.org/hco/17/GRCh38#38549176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97414403-C-A

38549176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97414403-C-T

38549342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414533-G-A

38549342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414533-G-T

38549348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414539-G-T

38549353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414544-C-T

38549356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414547-G-C

38549458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414649-T-A

38549517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414687-C-T

38549772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414888-C-T

38549880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97414984-C-T

38550141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97415205-A-G

38550263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97415288-G-A

38550323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97415333-T-C

38550965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97415997-G-A

http://identifiers.org/hco/17/GRCh38#38551035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97416062-C-A

38551035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416062-C-T

http://identifiers.org/hco/17/GRCh38#38551047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97416074-C-A

38551047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416074-C-T

http://identifiers.org/hco/17/GRCh38#38551057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97416084-A-C

38551057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416084-A-G

38551057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416084-A-T

http://identifiers.org/hco/17/GRCh38#38551098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97416123-C-A

38551098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416123-C-T

38551103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416128-G-A

38551103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416128-G-T

38551273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97416285-C-T

38551339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97416351-A-G

38551384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97416396-T-G

38551406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416412-G-A

38551406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416412-G-C

38551406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416412-G-T

http://identifiers.org/hco/17/GRCh38#38551449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97416462-C-A

38551449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416462-C-T

http://identifiers.org/hco/17/GRCh38#38551555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97416547-C-A

38551555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416547-C-T

38551569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416562-G-T

38551580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97416573-C-T

38551711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416696-G-A

38551711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416696-G-C

38551711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416696-G-T

38551723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416708-T-A

38551723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416708-T-C

38551804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416768-G-A

38551851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97416809-C-T

38552018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97416966-G-T

http://identifiers.org/hco/17/GRCh38#38552193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97417131-A-C

38552193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417131-A-G

http://identifiers.org/hco/17/GRCh38#38552196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97417134-C-A

38552242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417176-G-T

http://identifiers.org/hco/17/GRCh38#38552249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97417183-C-A

38552249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417183-C-T

38552311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417235-A-G

38552311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417235-A-T

http://identifiers.org/hco/17/GRCh38#38552333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97417257-C-A

38552333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417257-C-G

38552358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417283-G-C

38552358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417283-G-T

http://identifiers.org/hco/17/GRCh38#38552412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97417320-A-C

38552430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417338-G-A

38552430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417338-G-T

38552436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417344-G-A

38552436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417344-G-T

38552551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97417459-G-A

38552551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97417459-G-C

38552551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97417459-G-T

http://identifiers.org/hco/17/GRCh38#38552707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97417592-C-A

38552707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417592-C-G

38552707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417592-C-T

38552761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97417644-G-A

38552883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417768-C-T

38552984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417863-G-A

38552984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97417863-G-T

38553375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97418403-C-T

38553493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97418517-A-G

38553493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97418517-A-T

38553576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97418580-C-G

38554776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97419184-T-C

38554865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97419300-G-A

38555091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97419525-C-T

38555252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97419857-C-T

38555312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97419912-C-G

38555349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97419948-A-T

38555420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420027-T-C

http://identifiers.org/hco/17/GRCh38#38555504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97420082-A-C

38556300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420734-C-G

38556300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420734-C-T

38556352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420803-C-T

38556376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420825-G-T

38556430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420870-G-A

38556430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97420870-G-T

38556692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421088-G-A

http://identifiers.org/hco/17/GRCh38#38556733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97421129-C-A

38557220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421632-G-A

38557220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421632-G-C

38557220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421632-G-T

38557284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421690-C-T

38557289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421695-T-C

38557315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97421724-T-G

38557809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422192-C-T

38557877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422261-C-T

38558088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422451-G-A

38558088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422451-G-T

http://identifiers.org/hco/17/GRCh38#38558210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97422598-C-A

38558370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97422773-C-G

38558379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97422782-G-A

38558379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97422782-G-C

38558379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97422782-G-T

38558409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 97422812-G-A

38558409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 97422812-G-T

38558412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422815-G-A

38558412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422815-G-T

http://identifiers.org/hco/17/GRCh38#38558466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97422855-C-A

38558466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422855-C-G

38558466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422855-C-T

38558507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422895-G-A

38558507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422895-G-T

38558543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422932-G-A

38558543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422932-G-C

38558543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422932-G-T

38558581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97422970-G-A

38558662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423021-G-A

38558736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423092-G-T

38558885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423243-G-A

38558885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423243-G-T

38558904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423260-C-G

http://identifiers.org/hco/17/GRCh38#38558935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97423288-C-A

38558952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423302-T-G

38558953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423303-G-A

38558953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423303-G-T

38558959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423309-T-G

38559024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423357-T-G

38559113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423449-G-A

http://identifiers.org/hco/17/GRCh38#38559167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97423503-C-A

38559175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423511-A-G

38559245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423559-G-A

http://identifiers.org/hco/17/GRCh38#38559254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97423568-C-A

38559254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423568-C-G

38559266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423580-G-A

38559266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423580-G-T

38559334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423626-A-G

38559334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423626-A-T

38559343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423635-T-G

38559346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423638-G-C

38559346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423638-G-T

38559373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423650-T-C

38559373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423650-T-G

38559374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423651-G-A

38559374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423651-G-T

38559418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423683-G-A

38559418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423683-G-T

38559427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423692-G-A

38559427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423692-G-T

38559432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423697-A-G

38559432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423697-A-T

38559451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423716-G-A

38559451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97423716-G-C

38559546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423799-G-A

38559546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423799-G-T

38559560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423813-G-A

38559560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423813-G-C

38559560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423813-G-T

38559571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423834-G-A

38559571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97423834-G-T

38559580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97423843-G-A

38559651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97423914-G-A

38559651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97423914-G-C

38559651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97423914-G-T

38559689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97423952-G-T

38559693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97423956-T-C

38559693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97423956-T-G

38559771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 97424034-G-A

38559771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 97424034-G-T

38559774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 97424037-T-C

http://identifiers.org/hco/17/GRCh38#38559833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97424094-C-A

38559833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424094-C-T

38559999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424241-G-A

38559999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424241-G-T

38560021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424263-G-A

38560021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424263-G-T

38560082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97424319-G-A

38560082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97424319-G-T

http://identifiers.org/hco/17/GRCh38#38560135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97424376-C-A

38560135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424376-C-T

38560146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424387-C-T

38560206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424442-A-G

38560244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424476-A-G

38560296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424528-C-T

http://identifiers.org/hco/17/GRCh38#38560301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97424533-C-A

38560318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424549-G-A

38560318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424549-G-T

38560326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97424571-G-T

http://identifiers.org/hco/17/GRCh38#38560327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97424572-C-A

http://identifiers.org/hco/17/GRCh38#38560448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97424691-C-A

38560448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97424691-C-T

http://identifiers.org/hco/17/GRCh38#38560454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#97424697-C-A

38560454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97424697-C-G

38560454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97424697-C-T

38560659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424810-C-T

38560796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424875-G-A

38560802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97424881-G-T

38560946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97424956-C-T

38561192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97425097-T-C

38561213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97425118-T-C

38561217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97425122-C-T

http://identifiers.org/hco/17/GRCh38#38561324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97425183-C-A

38561390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97425194-G-A

38561390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97425194-G-C

38561390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97425194-G-T

38561507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425301-C-T

38561543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425337-A-T

38561564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425358-G-T

38561645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425439-G-A

38561645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425439-G-T

http://identifiers.org/hco/17/GRCh38#38561669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97425463-C-A

38561669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425463-C-G

38561669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425463-C-T

38561678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425472-G-A

38561678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 97425472-G-T

http://identifiers.org/hco/17/GRCh38#38561696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97425490-C-A

38561696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425490-C-T

38561768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425562-G-A

38561777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425571-G-A

38561777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 97425571-G-T

38561836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425627-G-A

38561836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97425627-G-T

38561876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425667-G-A

38561876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425667-G-T

38561894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97425685-G-A

38561894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97425685-G-T

38561942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425733-A-G

38561963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425754-G-A

38561963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 97425754-G-T

38562083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425874-G-A

38562083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97425874-G-T

http://identifiers.org/hco/17/GRCh38#38562170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97425961-C-A

38562170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97425961-C-G

38562170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97425961-C-T

38562374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426166-A-G

38562374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426166-A-T

38562648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426410-G-A

38562648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426410-G-T

38562769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426502-G-A

38562769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426502-G-C

38562769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426502-G-T

38562839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97426572-G-A

38562839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97426572-G-T

38562896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97426629-G-T

38562965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426701-G-A

38562965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426701-G-T

38563051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97426850-C-T

http://identifiers.org/hco/17/GRCh38#38563182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97427001-C-A

38563182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427001-C-G

38563182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427001-C-T

http://identifiers.org/hco/17/GRCh38#38563187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97427006-C-A

38563187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427006-C-T

38563188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427007-G-A

38563188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427007-G-C

38563188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427007-G-T

38563194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427013-G-A

38563194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427013-G-T

38563219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427034-G-T

38563227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427042-G-T

38563249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427064-G-A

38563249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427064-G-T

38563283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427096-G-A

38563283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427096-G-C

38563283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427096-G-T

38563311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427122-G-A

38563311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427122-G-C

38563311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427122-G-T

http://identifiers.org/hco/17/GRCh38#38563316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97427127-C-A

38563316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97427127-C-T

38563346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97427157-G-A

38563346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97427157-G-T

38563352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97427163-G-A

38563352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97427163-G-C

38563352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97427163-G-T

38563382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97427193-A-G

http://identifiers.org/hco/17/GRCh38#38563418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97427229-C-A

38563418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97427229-C-G

38563418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97427229-C-T

38563447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 97427258-G-A

38563537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97427348-C-T

38563567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97427378-G-A

38563572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97427383-C-T

38563580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 97427391-A-G

38563652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97427463-G-C

38563652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97427463-G-T

38563653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97427464-T-A

38563653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97427464-T-G

http://identifiers.org/hco/17/GRCh38#38563697-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97427503-A-C

38563697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97427503-A-G

38563766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97427560-T-C

38563766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97427560-T-G

38563881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97427649-G-A

http://identifiers.org/hco/17/GRCh38#38563898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97427666-A-C

38563985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97427745-G-T

38564036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427795-T-G

38564092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427844-G-A

38564092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427844-G-T

38564107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427859-G-A

38564107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97427859-G-T

38564362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97428115-T-A

38564362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97428115-T-C

38564362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97428115-T-G

38564413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97428166-C-T

http://identifiers.org/hco/17/GRCh38#38564441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97428226-C-A

38564837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97428626-C-T

38564937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97428702-T-C

http://identifiers.org/hco/17/GRCh38#38565238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97429060-C-A

38565395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97429767-T-C

http://identifiers.org/hco/17/GRCh38#38565536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97430065-A-C

38565868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97430533-A-G

http://identifiers.org/hco/17/GRCh38#38565902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97430561-C-A

38566144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97430786-T-G

38566239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431159-G-A

38566289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431202-C-T

38566319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431254-T-G

38566323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431258-C-T

38566355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431290-C-T

38566412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431444-A-G

38566826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97431948-A-G

38567572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97432693-G-A

38567669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97432836-G-A

38567788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97432937-G-A

38567814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97432947-G-A

38567934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97433075-C-T

38568143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97433294-G-A

http://identifiers.org/hco/17/GRCh38#38568332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97433469-C-A

38568334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97433471-A-G

38568604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97433831-T-C

38568664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97433890-G-A

38568664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97433890-G-C

38568888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434067-A-G

38568890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434069-C-G

38569271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434370-G-A

38569271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434370-G-T

38569454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434553-G-A

38569485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434584-G-A

38569485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434584-G-T

38569822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97434726-G-T

38570398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97435230-G-A

38570403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97435235-C-T

38570754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97435792-G-T

38571207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97436232-G-A

http://identifiers.org/hco/17/GRCh38#38571536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97436565-C-A

38571778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97436840-G-A

38571778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97436840-G-C

38571977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97437061-G-A

38572216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97437276-G-C

38572531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97437594-C-T

38572731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437768-G-T

38572764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437802-T-C

http://identifiers.org/hco/17/GRCh38#38572797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97437826-C-A

38572797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437826-C-T

38572819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437848-G-A

38572819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437848-G-T

http://identifiers.org/hco/17/GRCh38#38572820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97437849-C-A

38572820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437849-C-G

38572820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97437849-C-T

http://identifiers.org/hco/17/GRCh38#38572847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97437876-C-A

38572861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97437890-G-A

38572861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97437890-G-T

38572934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97437961-T-C

http://identifiers.org/hco/17/GRCh38#38572967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97437994-A-C

38572967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97437994-A-G

38573382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97438366-C-T

38573427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97438411-G-A

38573745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97438691-C-T

38573837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97438788-C-T

38574043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97438993-A-G

38574603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439438-A-G

38574618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439453-T-A

http://identifiers.org/hco/17/GRCh38#38574750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97439589-C-A

38574750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439589-C-T

38574786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439621-C-T

http://identifiers.org/hco/17/GRCh38#38574828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97439664-C-A

38574828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439664-C-T

38575014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439844-G-A

38575014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439844-G-C

38575014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439844-G-T

38575048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439877-G-A

38575048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439877-G-T

38575161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97439974-G-A

38576623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97440695-T-A

38576645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97440735-T-C

38576679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97440774-A-G

38577033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441224-T-A

38577073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441256-C-T

38577187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441396-A-G

http://identifiers.org/hco/17/GRCh38#38577218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97441427-C-A

38577266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441470-C-T

38577336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441517-A-G

38577490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441675-G-A

38577635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441808-G-A

38577661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441834-C-T

38577787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441939-G-A

38577787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97441939-G-T

38577952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442090-G-A

http://identifiers.org/hco/17/GRCh38#38577996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442130-C-A

38577996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442130-C-T

38578021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442152-C-T

http://identifiers.org/hco/17/GRCh38#38578345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442423-C-A

http://identifiers.org/hco/17/GRCh38#38578359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442433-C-A

38578359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442433-C-G

38578359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442433-C-T

http://identifiers.org/hco/17/GRCh38#38578438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442469-C-A

38578445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442476-G-A

38578445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442476-G-C

38578449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442480-G-A

38578449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442480-G-T

38578469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442484-C-G

38578469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442484-C-T

38578532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442545-G-A

38578532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: missense variant
orthologous variants: 97442545-G-T

38578592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442605-C-T

38578607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442620-G-A

38578655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442668-G-A

38578655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442668-G-C

38578655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442668-G-T

http://identifiers.org/hco/17/GRCh38#38578670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442683-C-A

http://identifiers.org/hco/17/GRCh38#38578703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442716-C-A

38578703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442716-C-T

http://identifiers.org/hco/17/GRCh38#38578757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442770-C-A

38578757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: synonymous variant
orthologous variants: 97442770-C-T

38578810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442823-G-A

38578810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442823-G-T

http://identifiers.org/hco/17/GRCh38#38578823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442833-A-C

38578823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442833-A-G

http://identifiers.org/hco/17/GRCh38#38578831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97442841-C-A

38578831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442841-C-T

38578875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442886-G-T

38578880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442891-G-A

38578880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97442891-G-T

38579434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97443343-A-G

38579450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97443363-C-T

38579455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97443368-C-T

38579581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97443490-C-T

38579692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97443588-A-G

38579749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97443644-G-T

38579976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97443831-A-G

38580066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97443922-G-A

38580217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97444072-T-G

38581483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97445677-A-T

http://identifiers.org/hco/17/GRCh38#38581515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97445709-C-A

http://identifiers.org/hco/17/GRCh38#38581675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97445872-C-A

38581675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97445872-C-T

38581692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97445895-C-G

38581740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97445960-C-T

38581808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446022-A-G

38581884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446049-A-G

http://identifiers.org/hco/17/GRCh38#38581895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97446060-C-A

38581895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446060-C-T

38582006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446156-C-T

38582018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446168-G-A

38582218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446505-C-T

38582256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446554-G-A

38582275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446573-G-A

38582282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446580-G-A

38582520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97446800-C-T

http://identifiers.org/hco/17/GRCh38#38582521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97446801-C-A

http://identifiers.org/hco/17/GRCh38#38584794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97448332-C-A

38584799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97448337-G-A

38585057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97448509-T-C

38585249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97448667-G-T

38585840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97449244-G-A

38585840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97449244-G-C

38585853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97449252-G-A

38585853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97449252-G-C

38585976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97449359-C-T

http://identifiers.org/hco/17/GRCh38#38586585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97449864-C-A

38586585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97449864-C-G

38586863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97450092-T-C

http://identifiers.org/hco/17/GRCh38#38587619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97450929-C-A

38587619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97450929-C-G

38587715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97451007-G-A

38587715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97451007-G-C

38587777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97451076-C-T

38587830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97451132-T-C

http://identifiers.org/hco/17/GRCh38#38588369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97451664-A-C

38588521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97451837-G-A

38589915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97452834-G-C

38589961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97452857-C-T

38589962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97452858-A-G

http://identifiers.org/hco/17/GRCh38#38590184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97453046-A-C

38590732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97453699-C-T

38590774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97453724-T-C

38591338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454111-G-C

38591429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454200-T-C

38591784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454499-G-A

38591789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454504-T-C

38591857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454540-G-A

38591857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454540-G-C

38592058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97454733-C-T

http://identifiers.org/hco/17/GRCh38#38594128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97456072-C-A

38594491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97456423-T-C

38594533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97456483-C-T

38595037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97456895-C-G

38595483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97457117-T-C

38595779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97457293-T-C

38595815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97457319-C-T

http://identifiers.org/hco/17/GRCh38#38595995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97457468-C-A

38596035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97457509-G-A

38596344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97457749-C-T

38596731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97458126-G-A

38597249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97458594-C-T

38597707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97458979-C-T

38598123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97459381-G-A

38598183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97459397-G-A

38598290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97459438-G-A

38598449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97459498-T-G

38598802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97459737-T-C

38598934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97459805-C-T

http://identifiers.org/hco/17/GRCh38#38599451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97460240-A-C

38600150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97460748-T-C

38600337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97460919-G-C

38600592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97461144-A-G

38600949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97461470-A-G

38601054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97461575-G-A

38601054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97461575-G-T

38601192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97461705-C-T

38601437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97461899-G-A

38601623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97462082-C-T

38601917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97462376-G-A

http://identifiers.org/hco/17/GRCh38#38602105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97462531-C-A

http://identifiers.org/hco/17/GRCh38#38602318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97462749-C-A

http://identifiers.org/hco/17/GRCh38#38602358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97462789-C-A

38602358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97462789-C-T

http://identifiers.org/hco/17/GRCh38#38602436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97462866-C-A

http://identifiers.org/hco/17/GRCh38#38602555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97462958-C-A

38602555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97462958-C-T

38602664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97463058-T-C

38602671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97463065-C-T

38602733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97463124-G-A

38602733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97463124-G-T

http://identifiers.org/hco/17/GRCh38#38602819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97463233-C-A

38602819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97463233-C-T

38603205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97463560-G-C

38603605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97463857-A-G

38603834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97464047-T-A

38603834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97464047-T-C

38603835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97464048-C-G

38604021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97464233-G-A

38604026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97464238-G-A

38604536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant
orthologous variants: 97464679-C-T

http://identifiers.org/hco/17/GRCh38#38604597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97464740-C-A

38604597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 97464740-C-T

38604628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97464770-G-A

http://identifiers.org/hco/17/GRCh38#38604681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97464823-A-C

38604838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97464981-C-T

38605069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97465214-G-A

38605267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97465402-T-C

38605301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97465436-C-T

http://identifiers.org/hco/17/GRCh38#38605779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#97465889-C-A

38605779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97465889-C-T

38605783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97465893-G-A

38605783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97465893-G-T

38605796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97465906-C-G

38605796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97465906-C-T

38605799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97465909-G-A

38605799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97465909-G-C

38605799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97465909-G-T

http://identifiers.org/hco/17/GRCh38#38605924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#97466035-C-A

38605924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97466035-C-T

38605926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97466037-A-T

38605928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97466039-T-C

38605928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97466039-T-G

38606438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97466573-C-G

38606438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97466573-C-T

38606446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97466581-C-T

38606448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron variant
orthologous variants: 97466583-G-A

38606543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: intron_variant, undefined
orthologous variants: 97466710-C-T

38606796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5 prime UTR variant
orthologous variants: 97466950-G-A

38606821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29506
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 97466963-G-C