13388155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112914979-C-G

13388155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112914979-C-T

13388263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915089-A-G

13388385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915206-A-G

13388472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915290-T-G

13388477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915295-T-C

13388522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915340-G-A

13388522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915340-G-T

13388527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915346-T-A

13388527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915346-T-C

13388527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915346-T-G

13388546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915365-G-T

13388555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915374-G-A

13388555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915374-G-C

13388555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915374-G-T

13388629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915449-G-A

13388750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915558-G-T

13388822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 112915627-A-G

13388868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 112915673-C-T

13388999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 112915804-T-C

13389172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112915974-G-A

http://identifiers.org/hco/11/GRCh38#13389229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112916038-C-A

13389229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916038-C-G

13389229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916038-C-T

13389794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916194-C-T

13389939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916325-C-T

13389962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916345-C-T

13389983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916363-A-G

13389987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112916367-A-G

http://identifiers.org/hco/11/GRCh38#13403043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112921782-C-A

13403087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112921829-T-C

http://identifiers.org/hco/11/GRCh38#13403119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112921852-C-A

13403119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112921852-C-T

13403414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112922135-T-A

13403414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112922135-T-C

13403463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112922184-G-A

13404653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 112924031-G-T

13404702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112924086-A-G

13404817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112924248-T-C

http://identifiers.org/hco/11/GRCh38#13405065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112924487-A-C

http://identifiers.org/hco/11/GRCh38#13405192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112924627-C-A

13405315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112924689-T-A

13405315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 112924689-T-G

http://identifiers.org/hco/11/GRCh38#13405569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112924871-C-A

http://identifiers.org/hco/11/GRCh38#13405618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112924943-C-A

13405618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112924943-C-T

13405626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112924953-T-C

http://identifiers.org/hco/11/GRCh38#13410614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112925758-C-A

13410639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112925779-T-C

13413131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112927010-T-C

13413380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112927423-G-T

http://identifiers.org/hco/11/GRCh38#13413395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112927438-C-A

13413406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112927449-T-C

13413406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112927449-T-G

http://identifiers.org/hco/11/GRCh38#13413413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112927456-C-A

http://identifiers.org/hco/11/GRCh38#13413606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112927622-A-C

http://identifiers.org/hco/11/GRCh38#13413707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112927719-C-A

13413767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112927778-G-T

13416536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928832-T-G

13417020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928948-A-T

13417035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928963-T-A

13417035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928963-T-C

13417035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928963-T-G

13417050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928978-T-A

13417050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928978-T-C

13417070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928981-G-A

13417070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928981-G-T

13417077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112928988-T-G

13417130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112929032-T-A

13417130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112929032-T-C

13417260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 112929164-C-T

13417275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112929179-A-G

http://identifiers.org/hco/11/GRCh38#13417307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112929193-C-A

13417307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112929193-C-T

13417357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112929243-T-A

http://identifiers.org/hco/11/GRCh38#13417538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112929441-A-C

http://identifiers.org/hco/11/GRCh38#13418040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112930444-C-A

13418322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112930717-C-T

13418544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112930905-C-T

http://identifiers.org/hco/11/GRCh38#13419003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112931346-C-A

13419003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112931346-C-T

http://identifiers.org/hco/11/GRCh38#13419004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112931347-A-C

13419004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112931347-A-G

13419004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112931347-A-T

http://identifiers.org/hco/11/GRCh38#13419035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112931378-C-A

13419093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112931431-G-T

http://identifiers.org/hco/11/GRCh38#13419344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112931687-C-A

13419366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112931713-T-C

13419480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112931837-C-G

13419534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112931891-T-C

13419534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112931891-T-G

13419847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112932351-T-A

http://identifiers.org/hco/11/GRCh38#13419867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112932365-A-C

13419867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112932365-A-T

13420119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112932555-T-A

13420496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112933242-G-A

13421102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112933999-T-C

http://identifiers.org/hco/11/GRCh38#13421516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112934414-A-C

13421516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112934414-A-G

13421589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112934480-A-G

http://identifiers.org/hco/11/GRCh38#13421910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112934802-C-A

13421910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112934802-C-T

13421952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112934844-G-A

13421952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112934844-G-T

http://identifiers.org/hco/11/GRCh38#13421966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112934858-C-A

13422186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112935134-G-C

13422329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112935270-G-A

13423113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112935978-A-G

13423310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112936240-G-A

13423420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112936335-A-T

13423487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112936393-C-T

13423563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112936458-C-T

13423880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112936758-T-G

13424620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112937516-A-G

13430283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112941217-T-C

13431016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112941841-T-C

http://identifiers.org/hco/11/GRCh38#13431031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112941856-C-A

13431045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112941870-T-C

13431078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112941901-T-C

13431266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112942055-C-T

http://identifiers.org/hco/11/GRCh38#13431771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112942572-C-A

13431771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112942572-C-T

13431813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112942611-G-A

13438208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112944689-C-G

13439339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112945727-T-C

13439705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112946068-T-C

13439709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112946072-T-C

http://identifiers.org/hco/11/GRCh38#13439797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112946157-C-A

13439887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 112946242-C-T

13440086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112946441-C-T

13440126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 112946480-C-T

http://identifiers.org/hco/11/GRCh38#13440354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112946711-C-A

13440354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112946711-C-T

13440524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112946870-A-T

13440574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112946912-T-C

13441304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112947484-T-A

http://identifiers.org/hco/11/GRCh38#13442200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112948198-A-C

http://identifiers.org/hco/11/GRCh38#13442373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112948353-A-C

13442476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112948468-T-C

13443493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112949697-C-T

http://identifiers.org/hco/11/GRCh38#13443553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112949764-A-C

13443911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112949920-C-T

13444818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112950773-A-G

13444899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112950855-T-C

13444932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112950886-T-C

13445158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112951122-A-G

13445295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112951263-A-T

13445489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112951473-G-A

13445562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112951543-T-C

13445938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112951912-T-C

13445975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112951949-A-G

13446072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112952041-A-G

13446226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112952205-T-A

13448696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112952829-A-T

13449182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112953340-G-T

13451507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112955249-T-C

13451552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112955292-T-A

http://identifiers.org/hco/11/GRCh38#13453380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112955843-A-C

13453490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112955925-T-C

13455420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112957984-T-C

13455761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112958336-C-T

13456090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112959522-C-T

http://identifiers.org/hco/11/GRCh38#13458481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112961048-A-C

13458540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112961099-C-T

13458627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112961192-T-A

13458627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112961192-T-C

13458835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112961520-A-G

13458882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112961566-T-C

13459015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112961703-T-C

13459416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112963555-C-T

13459419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112963556-G-A

13459548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112963991-C-T

13459581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112964027-A-T

13459749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112964189-T-C

13460098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112964935-G-A

13460342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112965180-C-G

13460494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112965320-G-A

13460523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112965349-T-C

13460996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112965760-A-G

13461108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112966489-C-T

13461691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112967063-G-A

13461750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112967109-T-G

http://identifiers.org/hco/11/GRCh38#13461851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112967200-C-A

13461851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112967200-C-T

http://identifiers.org/hco/11/GRCh38#13461951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#112967292-C-A

13461951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 112967292-C-T

http://identifiers.org/hco/11/GRCh38#13462493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#112967834-C-A

13462739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112968106-G-T

13462808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112968179-A-G

13462892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112968250-G-A

13462892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112968250-G-T

13463130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112968437-T-C

13463131-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112968438-T-G

13463134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21445
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 112968441-G-T